Expanding the canvas of PRKN mutations in familial and early-onset Parkinson disease
Author:
Funder
Department of Biotechnology, New Delhi
Council of Scientific and Industrial Research, New Delhi
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference9 articles.
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3. Parkin disease: a phenotypic study of a large case series;Khan;Brain,2003
4. French Parkinson's disease genetics study group; european consortium on genetic susceptibility in Parkinson's disease. Association between early-onset Parkinson disease and mutations in the parkin gene;Lücking;N. Engl. J. Med.,2000
5. A systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease;Kilarski;Mov. Disord.,2012
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