Case report: A novel mutation of glial fibrillary acidic protein gene causing juvenile-onset Alexander disease: Alexander disease (AxD) is a rare inherited autosomal dominant (AD) disease with different clinical phenotypes…… #Neurology https://t.co/u3HnHYz
RT @FrontNeurol: New Research: Case report: A novel mutation of glial fibrillary acidic protein gene causing juvenile-onset Alexander disea…
New Research: Case report: A novel mutation of glial fibrillary acidic protein gene causing juvenile-onset Alexander disease: Alexander disease (AxD) is a rare inherited autosomal dominant (AD) disease with different clinical phenotypes… https://t.co/nv0fE