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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| Description | scientific article |
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author: Claudia Tarlarini Christian Lunetta Silvana Penco Lorena Mosca |
| Publication date | March 6, 2012 |
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