Germline PTPN13 mutations in patients with bone marrow failure and acute lymphoblastic leukemia

Houtan Moshiri; David A. Cabrera Riofrío; Yeon Jung Lim; Supanun Lauhasurayotin; Michal Manisterski; Ronit Elhasid; Francisco A. Bonilla; Santhosh Dhanraj; Richard N. Armstrong; Hongbing Li; Stephen W. Scherer; Angel Hernández-Hernández; Yigal Dror

doi:10.1038/s41375-022-01610-4

Germline PTPN13 mutations in patients with bone marrow failure and acute lymphoblastic leukemia

Houtan Moshiri, David A. Cabrera Riofrío, Yeon Jung Lim, Supanun Lauhasurayotin, Michal Manisterski, Ronit Elhasid, Francisco A. Bonilla, Santhosh Dhanraj, Richard N. Armstrong, Hongbing Li, Stephen W. Scherer, Angel Hernández-Hernández, Yigal Dror^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

Original language	English
Pages (from-to)	2132-2135
Number of pages	4
Journal	Leukemia
Volume	36
Issue number	8
DOIs	https://doi.org/10.1038/s41375-022-01610-4
State	Published - Aug 2022
Externally published	Yes

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10.1038/s41375-022-01610-4

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Moshiri, H., Cabrera Riofrío, D. A., Lim, Y. J., Lauhasurayotin, S., Manisterski, M., Elhasid, R., Bonilla, F. A., Dhanraj, S., Armstrong, R. N., Li, H., Scherer, S. W., Hernández-Hernández, A., & Dror, Y. (2022). Germline PTPN13 mutations in patients with bone marrow failure and acute lymphoblastic leukemia. Leukemia, 36(8), 2132-2135. https://doi.org/10.1038/s41375-022-01610-4

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title = "Germline PTPN13 mutations in patients with bone marrow failure and acute lymphoblastic leukemia",

author = "Houtan Moshiri and {Cabrera Riofr{\'i}o}, {David A.} and Lim, {Yeon Jung} and Supanun Lauhasurayotin and Michal Manisterski and Ronit Elhasid and Bonilla, {Francisco A.} and Santhosh Dhanraj and Armstrong, {Richard N.} and Hongbing Li and Scherer, {Stephen W.} and Angel Hern{\'a}ndez-Hern{\'a}ndez and Yigal Dror",

note = "Funding Information: The authors thank and acknowledge the patients and families for their participation in this study. Also, the authors would like to acknowledge the Care4Rare Research Consortium for identifying the mutation in the index case of Family A. The study was supported by grants from the Canadian Institutes of Health Research funding reference 286737 (YD), McLaughlin Centre Accelerator Grants in Genomic Medicine (YD and SWS), The Regional Government of Castile & Leon funding reference SA077P20 (AHH), and The Spanish Government funding reference PID2020–117692RB-I00 (AHH). The Care4Rare Canada Consortium work was funded by Genome Canada and the Ontario Genomics Institute (OGI147). ",

year = "2022",

month = aug,

doi = "10.1038/s41375-022-01610-4",

language = "אנגלית",

volume = "36",

pages = "2132--2135",

journal = "Leukemia",

issn = "0887-6924",

publisher = "Springer Nature",

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}

Moshiri, H, Cabrera Riofrío, DA, Lim, YJ, Lauhasurayotin, S, Manisterski, M, Elhasid, R, Bonilla, FA, Dhanraj, S, Armstrong, RN, Li, H, Scherer, SW, Hernández-Hernández, A & Dror, Y 2022, 'Germline PTPN13 mutations in patients with bone marrow failure and acute lymphoblastic leukemia', Leukemia, vol. 36, no. 8, pp. 2132-2135. https://doi.org/10.1038/s41375-022-01610-4

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T1 - Germline PTPN13 mutations in patients with bone marrow failure and acute lymphoblastic leukemia

AU - Moshiri, Houtan

AU - Cabrera Riofrío, David A.

AU - Lim, Yeon Jung

AU - Lauhasurayotin, Supanun

AU - Manisterski, Michal

AU - Elhasid, Ronit

AU - Bonilla, Francisco A.

AU - Dhanraj, Santhosh

AU - Armstrong, Richard N.

AU - Li, Hongbing

AU - Scherer, Stephen W.

AU - Hernández-Hernández, Angel

AU - Dror, Yigal

N1 - Funding Information: The authors thank and acknowledge the patients and families for their participation in this study. Also, the authors would like to acknowledge the Care4Rare Research Consortium for identifying the mutation in the index case of Family A. The study was supported by grants from the Canadian Institutes of Health Research funding reference 286737 (YD), McLaughlin Centre Accelerator Grants in Genomic Medicine (YD and SWS), The Regional Government of Castile & Leon funding reference SA077P20 (AHH), and The Spanish Government funding reference PID2020–117692RB-I00 (AHH). The Care4Rare Canada Consortium work was funded by Genome Canada and the Ontario Genomics Institute (OGI147).

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VL - 36

SP - 2132

EP - 2135

JO - Leukemia

JF - Leukemia

IS - 8

ER -

Germline PTPN13 mutations in patients with bone marrow failure and acute lymphoblastic leukemia

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