Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery (European Journal of Human Genetics, (2020), 28, 8, (1034-1043), 10.1038/s41431-020-0609-9)

Holger Hengel; Rebecca Buchert; Marc Sturm; Tobias B. Haack; Yvonne Schelling; Muhammad Mahajnah; Rajech Sharkia; Abdussalam Azem; Ghassan Balousha; Zaid Ghanem; Mohammed Falana; Osama Balousha; Suhail Ayesh; Reinhard Keimer; Werner Deigendesch; Jimmy Zaidan; Hiyam Marzouqa; Peter Bauer; Ludger Schöls

doi:10.1038/s41431-021-00909-7

Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery (European Journal of Human Genetics, (2020), 28, 8, (1034-1043), 10.1038/s41431-020-0609-9)

Holger Hengel, Rebecca Buchert, Marc Sturm, Tobias B. Haack, Yvonne Schelling, Muhammad Mahajnah, Rajech Sharkia, Abdussalam Azem, Ghassan Balousha, Zaid Ghanem, Mohammed Falana, Osama Balousha, Suhail Ayesh, Reinhard Keimer, Werner Deigendesch, Jimmy Zaidan, Hiyam Marzouqa, Peter Bauer, Ludger Schöls^*

^*Corresponding author for this work

Biochemistry Molecular Biology

Research output: Contribution to journal › Comment/debate

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Abstract

The article “First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery,” written by Holger Hengel et al., was originally published electronically on the publisher’s internet portal on 25 March 2020 without open access.

Original language	English
Pages (from-to)	248
Number of pages	1
Journal	European Journal of Human Genetics
Volume	30
Issue number	2
DOIs	https://doi.org/10.1038/s41431-021-00909-7
State	Published - Feb 2022

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Hengel, H., Buchert, R., Sturm, M., Haack, T. B., Schelling, Y., Mahajnah, M., Sharkia, R., Azem, A., Balousha, G., Ghanem, Z., Falana, M., Balousha, O., Ayesh, S., Keimer, R., Deigendesch, W., Zaidan, J., Marzouqa, H., Bauer, P., & Schöls, L. (2022). Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery (European Journal of Human Genetics, (2020), 28, 8, (1034-1043), 10.1038/s41431-020-0609-9). European Journal of Human Genetics, 30(2), 248. https://doi.org/10.1038/s41431-021-00909-7

Hengel, Holger ; Buchert, Rebecca ; Sturm, Marc et al. / Correction to : First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery (European Journal of Human Genetics, (2020), 28, 8, (1034-1043), 10.1038/s41431-020-0609-9). In: European Journal of Human Genetics. 2022 ; Vol. 30, No. 2. pp. 248.

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title = "Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery (European Journal of Human Genetics, (2020), 28, 8, (1034-1043), 10.1038/s41431-020-0609-9)",

abstract = "The article “First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery,” written by Holger Hengel et al., was originally published electronically on the publisher{\textquoteright}s internet portal on 25 March 2020 without open access.",

author = "Holger Hengel and Rebecca Buchert and Marc Sturm and Haack, {Tobias B.} and Yvonne Schelling and Muhammad Mahajnah and Rajech Sharkia and Abdussalam Azem and Ghassan Balousha and Zaid Ghanem and Mohammed Falana and Osama Balousha and Suhail Ayesh and Reinhard Keimer and Werner Deigendesch and Jimmy Zaidan and Hiyam Marzouqa and Peter Bauer and Ludger Sch{\"o}ls",

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doi = "10.1038/s41431-021-00909-7",

language = "אנגלית",

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Hengel, H, Buchert, R, Sturm, M, Haack, TB, Schelling, Y, Mahajnah, M, Sharkia, R, Azem, A, Balousha, G, Ghanem, Z, Falana, M, Balousha, O, Ayesh, S, Keimer, R, Deigendesch, W, Zaidan, J, Marzouqa, H, Bauer, P & Schöls, L 2022, 'Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery (European Journal of Human Genetics, (2020), 28, 8, (1034-1043), 10.1038/s41431-020-0609-9)', European Journal of Human Genetics, vol. 30, no. 2, pp. 248. https://doi.org/10.1038/s41431-021-00909-7

Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery (European Journal of Human Genetics, (2020), 28, 8, (1034-1043), 10.1038/s41431-020-0609-9). / Hengel, Holger; Buchert, Rebecca; Sturm, Marc et al.
In: European Journal of Human Genetics, Vol. 30, No. 2, 02.2022, p. 248.

Research output: Contribution to journal › Comment/debate

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AU - Hengel, Holger

AU - Buchert, Rebecca

AU - Sturm, Marc

AU - Haack, Tobias B.

AU - Schelling, Yvonne

AU - Mahajnah, Muhammad

AU - Sharkia, Rajech

AU - Azem, Abdussalam

AU - Balousha, Ghassan

AU - Ghanem, Zaid

AU - Falana, Mohammed

AU - Balousha, Osama

AU - Ayesh, Suhail

AU - Keimer, Reinhard

AU - Deigendesch, Werner

AU - Zaidan, Jimmy

AU - Marzouqa, Hiyam

AU - Bauer, Peter

AU - Schöls, Ludger

PY - 2022/2

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Hengel H, Buchert R, Sturm M, Haack TB, Schelling Y, Mahajnah M et al. Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery (European Journal of Human Genetics, (2020), 28, 8, (1034-1043), 10.1038/s41431-020-0609-9). European Journal of Human Genetics. 2022 Feb;30(2):248. doi: 10.1038/s41431-021-00909-7

Correction to: First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery (European Journal of Human Genetics, (2020), 28, 8, (1034-1043), 10.1038/s41431-020-0609-9)

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