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Activation of a Cryptic Splice Site of GFAP in a Patient With Adult-Onset Alexander Disease.

Eiichiro AmanoTomokatsu YoshidaIkuko MizutaJun OyamaShingo SakashitaSyunsuke UeyamaAkira MachidaTakanori Yokota
Published in: Neurology. Genetics (2021)
GFAP gene expression analysis is necessary to clarify the effects of intronic mutations on splicing, even if they are in canonical splice sites. This case showed a much milder phenotype than those in previous cases with missense mutations at Glu207, thereby expanding the clinical spectrum of ALXDRD with Glu207 mutation.
Keyphrases
  • genome wide identification
  • case report
  • genome wide
  • copy number
  • intellectual disability
  • dna methylation
  • autism spectrum disorder
  • genome wide analysis