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


  • Human Mutation, 41, 1131–1137 (2020) 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