Genome-wide estimate of the heritability of Multiple System Atrophy

INTRODUCTION: Multiple System Atrophy (MSA) is a neurodegenerative disease which presents heterogeneously with symptoms and signs of parkinsonism, ataxia and autonomic dysfunction. Although MSA typically occurs sporadically, rare pathology-proven MSA families following either autosomal recessive or...

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Vydáno v:Parkinsonism Relat Disord
Hlavní autoři: Federoff, M, Price, TR, Sailer, A, Scholz, S, Hernandez, D, Nicolas, A, Singleton, AB, Nalls, M, Houlden, H
Médium: Artigo
Jazyk:Inglês
Vydáno: 2015
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4695377/
https://ncbi.nlm.nih.gov/pubmed/26589003
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2015.11.005
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