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Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes
Sudhaman, Sumedha, Muthane, Uday B, Behari, Madhuri, Govindappa, Shyla T, Juyal, Ramesh C, Thelma, B KVolume:
53
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmedgenet-2015-103616
Date:
August, 2016
File:
PDF, 1.02 MB
english, 2016