Genome-wide estimate of the heritability of Multiple System Atrophy.
Federoff M, Price TR, Sailer A et al.
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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 autosomal dominant patterns have been described, indicating a heritable contribution to the pathogenesis.
907 European ancestry cases, 3,866 European ancestry controls
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