Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS)

Twelve cases of adult-onset progressive muscular atrophy variant of amyotrophic lateral sclerosis (PMA/ALS) were studied in a small rural population of 1500 in the Republic of Belarus (former Soviet Union). The patients were members of three apparently related kindreds, each showing autosomal domina...

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Veröffentlicht in:	Journal of the neurological sciences 2000-08, Vol.177 (2), p.124-130
Hauptverfasser:	Cervenakova, Larisa, Protas, Iosif I, Hirano, Asao, Votiakov, Veniamin I, Nedzved, Mikhail K, Kolomiets, Natalia D, Taller, Inna, Park, Kye-Yoon, Sambuughin, Nyamkhishig, Gajdusek, D.Carleton, Brown, Paul, Goldfarb, Lev G
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Age of Onset Amyotrophic Lateral Sclerosis - genetics Amyotrophic Lateral Sclerosis - pathology Belarus Biological and medical sciences D101N mutation Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Familial amyotrophic lateral sclerosis Female Humans Male Medical sciences Middle Aged Muscular Atrophy, Spinal - genetics Muscular Atrophy, Spinal - pathology Neurology Pedigree Phenotype Republic of Belarus Rural Population SOD1 gene Spinal Cord - pathology Superoxide Dismutase - genetics
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