Erratum: Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number (American Journal of Human Genetics (2016) 99(4) (860–876) (S0002929716303391) (10.1016/j.ajhg.2016.08.014))

Kyle Thompson; Homa Majd; Cristina Dallabona; Karit Reinson; Martin S. King; Charlotte L. Alston; Langping He; Tiziana Lodi; Simon A. Jones; Aviva Fattal-Valevski; Nitay D. Fraenkel; Ann Saada; Alon Haham; Pirjo Isohanni; Roshni Vara; Inês A. Barbosa; Michael A. Simpson; Charu Deshpande; Sanna Puusepp; Penelope E. Bonnen; Richard J. Rodenburg; Anu Suomalainen; Katrin Õunap; Orly Elpeleg; Ileana Ferrero; Robert McFarland; Edmund R.S. Kunji; Robert W. Taylor

doi:10.1016/j.ajhg.2016.11.001

Erratum: Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number (American Journal of Human Genetics (2016) 99(4) (860–876) (S0002929716303391) (10.1016/j.ajhg.2016.08.014))

Kyle Thompson, Homa Majd, Cristina Dallabona, Karit Reinson, Martin S. King, Charlotte L. Alston, Langping He, Tiziana Lodi, Simon A. Jones, Aviva Fattal-Valevski, Nitay D. Fraenkel, Ann Saada, Alon Haham, Pirjo Isohanni, Roshni Vara, Inês A. Barbosa, Michael A. Simpson, Charu Deshpande, Sanna Puusepp, Penelope E. BonnenRichard J. Rodenburg, Anu Suomalainen, Katrin Õunap, Orly Elpeleg, Ileana Ferrero, Robert McFarland, Edmund R.S. Kunji, Robert W. Taylor^*

^*Corresponding author for this work

Clinical Departments

Research output: Contribution to journal › Comment/debate

Abstract

(The American Journal of Human Genetics 99, 860–876; October 6, 2016) In the originally published version of this article, Cristina Dallabona's first name was unfortunately misspelled. It appears correctly here and online. The authors regret the error.

Original language	English
Pages (from-to)	1405
Number of pages	1
Journal	American Journal of Human Genetics
Volume	99
Issue number	6
DOIs	https://doi.org/10.1016/j.ajhg.2016.11.001
State	Published - 1 Dec 2016

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Access to Document

10.1016/j.ajhg.2016.11.001

Fingerprint

Dive into the research topics of 'Erratum: Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number (American Journal of Human Genetics (2016) 99(4) (860–876) (S0002929716303391) (10.1016/j.ajhg.2016.08.014))'. Together they form a unique fingerprint.

Cite this

Thompson, K., Majd, H., Dallabona, C., Reinson, K., King, M. S., Alston, C. L., He, L., Lodi, T., Jones, S. A., Fattal-Valevski, A., Fraenkel, N. D., Saada, A., Haham, A., Isohanni, P., Vara, R., Barbosa, I. A., Simpson, M. A., Deshpande, C., Puusepp, S., ... Taylor, R. W. (2016). Erratum: Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number (American Journal of Human Genetics (2016) 99(4) (860–876) (S0002929716303391) (10.1016/j.ajhg.2016.08.014)). American Journal of Human Genetics, 99(6), 1405. https://doi.org/10.1016/j.ajhg.2016.11.001

Thompson, Kyle ; Majd, Homa ; Dallabona, Cristina et al. / Erratum : Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number (American Journal of Human Genetics (2016) 99(4) (860–876) (S0002929716303391) (10.1016/j.ajhg.2016.08.014)). In: American Journal of Human Genetics. 2016 ; Vol. 99, No. 6. pp. 1405.

@article{f9d6bf5b5c3f4d98bf7ad29875a4279f,

title = "Erratum: Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number (American Journal of Human Genetics (2016) 99(4) (860–876) (S0002929716303391) (10.1016/j.ajhg.2016.08.014))",

abstract = "(The American Journal of Human Genetics 99, 860–876; October 6, 2016) In the originally published version of this article, Cristina Dallabona's first name was unfortunately misspelled. It appears correctly here and online. The authors regret the error.",

author = "Kyle Thompson and Homa Majd and Cristina Dallabona and Karit Reinson and King, {Martin S.} and Alston, {Charlotte L.} and Langping He and Tiziana Lodi and Jones, {Simon A.} and Aviva Fattal-Valevski and Fraenkel, {Nitay D.} and Ann Saada and Alon Haham and Pirjo Isohanni and Roshni Vara and Barbosa, {In{\^e}s A.} and Simpson, {Michael A.} and Charu Deshpande and Sanna Puusepp and Bonnen, {Penelope E.} and Rodenburg, {Richard J.} and Anu Suomalainen and Katrin {\~O}unap and Orly Elpeleg and Ileana Ferrero and Robert McFarland and Kunji, {Edmund R.S.} and Taylor, {Robert W.}",

note = "Publisher Copyright: {\textcopyright} 2016 The Author(s)",

year = "2016",

month = dec,

day = "1",

doi = "10.1016/j.ajhg.2016.11.001",

language = "אנגלית",

volume = "99",

pages = "1405",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "6",

}

Thompson, K, Majd, H, Dallabona, C, Reinson, K, King, MS, Alston, CL, He, L, Lodi, T, Jones, SA, Fattal-Valevski, A, Fraenkel, ND, Saada, A, Haham, A, Isohanni, P, Vara, R, Barbosa, IA, Simpson, MA, Deshpande, C, Puusepp, S, Bonnen, PE, Rodenburg, RJ, Suomalainen, A, Õunap, K, Elpeleg, O, Ferrero, I, McFarland, R, Kunji, ERS & Taylor, RW 2016, 'Erratum: Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number (American Journal of Human Genetics (2016) 99(4) (860–876) (S0002929716303391) (10.1016/j.ajhg.2016.08.014))', American Journal of Human Genetics, vol. 99, no. 6, pp. 1405. https://doi.org/10.1016/j.ajhg.2016.11.001

Erratum: Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number (American Journal of Human Genetics (2016) 99(4) (860–876) (S0002929716303391) (10.1016/j.ajhg.2016.08.014)). / Thompson, Kyle; Majd, Homa; Dallabona, Cristina et al.
In: American Journal of Human Genetics, Vol. 99, No. 6, 01.12.2016, p. 1405.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Erratum

T2 - Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number (American Journal of Human Genetics (2016) 99(4) (860–876) (S0002929716303391) (10.1016/j.ajhg.2016.08.014))

AU - Thompson, Kyle

AU - Majd, Homa

AU - Dallabona, Cristina

AU - Reinson, Karit

AU - King, Martin S.

AU - Alston, Charlotte L.

AU - He, Langping

AU - Lodi, Tiziana

AU - Jones, Simon A.

AU - Fattal-Valevski, Aviva

AU - Fraenkel, Nitay D.

AU - Saada, Ann

AU - Haham, Alon

AU - Isohanni, Pirjo

AU - Vara, Roshni

AU - Barbosa, Inês A.

AU - Simpson, Michael A.

AU - Deshpande, Charu

AU - Puusepp, Sanna

AU - Bonnen, Penelope E.

AU - Rodenburg, Richard J.

AU - Suomalainen, Anu

AU - Õunap, Katrin

AU - Elpeleg, Orly

AU - Ferrero, Ileana

AU - McFarland, Robert

AU - Kunji, Edmund R.S.

AU - Taylor, Robert W.

PY - 2016/12/1

Y1 - 2016/12/1

N2 - (The American Journal of Human Genetics 99, 860–876; October 6, 2016) In the originally published version of this article, Cristina Dallabona's first name was unfortunately misspelled. It appears correctly here and online. The authors regret the error.

AB - (The American Journal of Human Genetics 99, 860–876; October 6, 2016) In the originally published version of this article, Cristina Dallabona's first name was unfortunately misspelled. It appears correctly here and online. The authors regret the error.

UR - http://www.scopus.com/inward/record.url?scp=85003955358&partnerID=8YFLogxK

U2 - 10.1016/j.ajhg.2016.11.001

DO - 10.1016/j.ajhg.2016.11.001

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.comment???

AN - SCOPUS:85003955358

SN - 0002-9297

VL - 99

SP - 1405

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 6

ER -

Thompson K, Majd H, Dallabona C, Reinson K, King MS, Alston CL et al. Erratum: Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number (American Journal of Human Genetics (2016) 99(4) (860–876) (S0002929716303391) (10.1016/j.ajhg.2016.08.014)). American Journal of Human Genetics. 2016 Dec 1;99(6):1405. doi: 10.1016/j.ajhg.2016.11.001

Erratum: Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number (American Journal of Human Genetics (2016) 99(4) (860–876) (S0002929716303391) (10.1016/j.ajhg.2016.08.014))

Abstract

UN SDGs

Access to Document

Other files and links

Fingerprint

Cite this