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Phenotypic variability of PINK1 expression: 12 Years' clinical follow-up of two Italian families.
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Mov Disord 2014 Aug;
Authors: Lucia Ricciardi, Simona Petrucci, Arianna Guidubaldi, Tamara Ialongo, Laura Serra, Alessandro Ferraris, Barbara SpanÚ, Marco Bozzali, Enza Maria Valente, Anna Rita Bentivoglio
Mutations in the PINK1 gene are the second most frequent cause of autosomal recessive early-onset parkinsonism.
PMID: 25164310 [PubMed - as supplied by publisher]