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Diagnostic exome sequencing in early‐onset Parkinson's disease confirms VPS13C as a rare cause of autosomal‐recessive Parkinson's disease.

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Title: Diagnostic exome sequencing in early‐onset Parkinson's disease confirms VPS13C as a rare cause of autosomal‐recessive Parkinson's disease.
Authors: Schormair, B.1,2, Kemlink, D.3, Mollenhauer, B.4,5, Fiala, O.3,6, Machetanz, G.4, Roth, J.3, Berutti, R.7, Strom, T. M.2,7, Haslinger, B.8, Trenkwalder, C.4, Zahorakova, D.9, Martasek, P.9, Ruzicka, E.3, Winkelmann, J.1,2,8,10 juliane.winkelmann@tum.de
Source: Clinical Genetics. Mar2018, Vol. 93 Issue 3, p603-612. 11p. 1 Diagram, 8 Charts.
Database: Academic Search Ultimate
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  Data: <searchLink fieldCode="JN" term="%22Clinical+Genetics%22">Clinical Genetics</searchLink>. Mar2018, Vol. 93 Issue 3, p603-612. 11p. 1 Diagram, 8 Charts.
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