Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject

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Title
Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject
Authors
Keywords
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Journal
NEUROBIOLOGY OF AGING
Volume 33, Issue 8, Pages 1846.e1-1846.e4
Publisher
Elsevier BV
Online
2012-03-06
DOI
10.1016/j.neurobiolaging.2012.01.108

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