Recessively‐Inherited Adult‐Onset Alexander Disease Caused by a Homozygous Mutation in the GFAP Gene
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DOI: 10.1002/mds.28099
Abstract: Alexander disease (AxD) is an autosomal‐dominant leukodystrophy caused by heterozygous mutations in the glial fibrillary acidic protein (GFAP) gene. read more here.
Keywords: alexander disease; recessively inherited; gfap gene;