Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease

Author:

Li Rong,Johnson Anne B.,Salomons Gajja,Goldman James E.,Naidu Sakkubai,Quinlan Roy,Cree Bruce,Ruyle Stephanie Z.,Banwell Brenda,D'Hooghe Marc,Siebert Joseph R.,Rolf Cristin M.,Cox Helen,Reddy Alyssa,Gutiérrez-Solana Luis González,Collins Amanda,Weller Roy O.,Messing Albee,van der Knaap Marjo S.,Brenner Michael

Funder

NIH (National Institute of Neurological Disorders and Stroke)

Mental Retardation Research Center

Lei Foundation

United Leukodystrophy Foundation

National Institute of Child Health and Human Development Brain and Tissue Bank for Developmental Disorders under National Institute of Child Health and Human Development

National Neurological Research Specimen Bank

National Institute of Neurological Disorders and Stroke/National Institute of Mental Health

National Multiple Sclerosis Society

Hereditary Disease Foundation

Veterans Health Services and Research Administration, Department of Veterans Affairs

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference90 articles.

1. Alexander's disease: a report and reappraisal;Russo;Neurology,1976

2. Alexander disease: new insights from genetics;Messing;J Neuropathol Exp Neurol,2001

3. Alexander disease: clinical, pathological and genetic features;Johnson;J Child Neurol,2003

4. Über eine eigenthümliche, mit Syringomyelie komplizierte Geschwulst des Rückenmarks;Rosenthal;(Bietr) Betrieb Pathol Anat,1898

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