Activation of a Cryptic Splice Site of GFAP in a Patient With Adult-Onset Alexander Disease.
Eiichiro AmanoTomokatsu YoshidaIkuko MizutaJun OyamaShingo SakashitaSyunsuke UeyamaAkira MachidaTakanori YokotaPublished 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.