PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism.
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Khodadadi H, et al. Among authors: aghamollaii v.
Mov Disord. 2017 Feb;32(2):287-291. doi: 10.1002/mds.26824. Epub 2016 Oct 18.
Mov Disord. 2017.
PMID: 27753167
Free PMC article.