Corrigendum to: Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform (Human Mutation, (2020), 41, 6, (1131-1137), 10.1002/humu.24008)

Guy Helman; Asako Takanohashi; Tracy L. Hagemann; Ming D. Perng; Marzena Walkiewicz; Sarah Woidill; Sunetra Sase; Zachary Cross; Yangzhu Du; Ling Zhao; Amy Waldman; Bret C. Haake; Ali Fatemi; Michael Brenner; Omar Sherbini; Albee Messing; Adeline Vanderver; Cas Simons

doi:10.1002/humu.24400

Corrigendum to: Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform (Human Mutation, (2020), 41, 6, (1131-1137), 10.1002/humu.24008)

Guy Helman, Asako Takanohashi, Tracy L. Hagemann, Ming D. Perng, Marzena Walkiewicz, Sarah Woidill, Sunetra Sase, Zachary Cross, Yangzhu Du, Ling Zhao, Amy Waldman, Bret C. Haake, Ali Fatemi, Michael Brenner, Omar Sherbini, Albee Messing, Adeline Vanderver, Cas Simons

Kennedy Krieger Institute

Research output: Contribution to journal › Comment/debate › peer-review

Abstract

Human Mutation, 41, 1131–1137 (2020) https://doi.org/10.1002/humu.24008 In this article published in June 2020, the authors describe exonic variants identified in three unrelated families with Type II Alexander disease that alter the splicing of GFAP pre-messenger RNA (mRNA) and result in the upregulation of a previously uncharacterized GFAP lambda isoform (NM_001363846.1). The authors would like to acknowledge further support of this study by the Commonwealth of Pennsylvania, Department of Health, Formula Grant, SAP 4100077047. The authors apologize for this omission.

Original language	English (US)
Pages (from-to)	1344
Number of pages	1
Journal	Human mutation
Volume	43
Issue number	9
DOIs	https://doi.org/10.1002/humu.24400
State	Published - Sep 2022

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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Helman, G., Takanohashi, A., Hagemann, T. L., Perng, M. D., Walkiewicz, M., Woidill, S., Sase, S., Cross, Z., Du, Y., Zhao, L., Waldman, A., Haake, B. C., Fatemi, A., Brenner, M., Sherbini, O., Messing, A., Vanderver, A., & Simons, C. (2022). Corrigendum to: Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform (Human Mutation, (2020), 41, 6, (1131-1137), 10.1002/humu.24008). Human mutation, 43(9), 1344. https://doi.org/10.1002/humu.24400

Corrigendum to: Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform (Human Mutation, (2020), 41, 6, (1131-1137), 10.1002/humu.24008). / Helman, Guy; Takanohashi, Asako; Hagemann, Tracy L. et al.
In: Human mutation, Vol. 43, No. 9, 09.2022, p. 1344.

Research output: Contribution to journal › Comment/debate › peer-review

Helman, G, Takanohashi, A, Hagemann, TL, Perng, MD, Walkiewicz, M, Woidill, S, Sase, S, Cross, Z, Du, Y, Zhao, L, Waldman, A, Haake, BC, Fatemi, A, Brenner, M, Sherbini, O, Messing, A, Vanderver, A & Simons, C 2022, 'Corrigendum to: Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform (Human Mutation, (2020), 41, 6, (1131-1137), 10.1002/humu.24008)', Human mutation, vol. 43, no. 9, pp. 1344. https://doi.org/10.1002/humu.24400

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abstract = "Human Mutation, 41, 1131–1137 (2020) https://doi.org/10.1002/humu.24008 In this article published in June 2020, the authors describe exonic variants identified in three unrelated families with Type II Alexander disease that alter the splicing of GFAP pre-messenger RNA (mRNA) and result in the upregulation of a previously uncharacterized GFAP lambda isoform (NM_001363846.1). The authors would like to acknowledge further support of this study by the Commonwealth of Pennsylvania, Department of Health, Formula Grant, SAP 4100077047. The authors apologize for this omission.",

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AU - Woidill, Sarah

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AU - Du, Yangzhu

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AB - Human Mutation, 41, 1131–1137 (2020) https://doi.org/10.1002/humu.24008 In this article published in June 2020, the authors describe exonic variants identified in three unrelated families with Type II Alexander disease that alter the splicing of GFAP pre-messenger RNA (mRNA) and result in the upregulation of a previously uncharacterized GFAP lambda isoform (NM_001363846.1). The authors would like to acknowledge further support of this study by the Commonwealth of Pennsylvania, Department of Health, Formula Grant, SAP 4100077047. The authors apologize for this omission.

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Corrigendum to: Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform (Human Mutation, (2020), 41, 6, (1131-1137), 10.1002/humu.24008)

Abstract

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