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)

Academic Article

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.
  • Authors

    Published In

  • Human Mutation  Journal
  • Digital Object Identifier (doi)

    Author List

  • Helman G; Takanohashi A; Hagemann TL; Perng MD; Walkiewicz M; Woidill S; Sase S; Cross Z; Du Y; Zhao L
  • Start Page

  • 1344
  • Volume

  • 43
  • Issue

  • 9