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PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism.

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Title: PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism.
Authors: Khodadadi, Hamidreza1, Azcona, Luis J.2,3, Aghamollaii, Vajiheh4, Omrani, Mir Davood1, Garshasbi, Masoud5, Taghavi, Shaghayegh1, Tafakhori, Abbas6, Shahidi, Gholam Ali7, Jamshidi, Javad8, Darvish, Hossein1, Paisán‐Ruiz, Coro3,9,10,11,12 coro.paisan-ruiz@mssm.edu, Paisán-Ruiz, Coro13,14,15,16,17 (AUTHOR)
Source: Movement Disorders. Feb2017, Vol. 32 Issue 2, p287-291. 6p.
Database: Academic Search Ultimate
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  Data: PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism.
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  Data: <searchLink fieldCode="JN" term="%22Movement+Disorders%22">Movement Disorders</searchLink>. Feb2017, Vol. 32 Issue 2, p287-291. 6p.
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        Value: 10.1002/mds.26824
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              Text: Feb2017
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