Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability.
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Santoro L, et al. Among authors: nolano m.
Neurogenetics. 2011 Feb;12(1):33-9. doi: 10.1007/s10048-010-0259-0. Epub 2010 Sep 21.
Neurogenetics. 2011.
PMID: 20853184
Free PMC article.