Early Onset Parkinson’s Disease in a family of Moroccan origin caused by a p.A217D mutation in PINK1: a case report
Norman, Brendan P., Lubbe, Steven J., Tan, Manuela, Warren, Naomi, Morris, Huw R.Volume:
17
Language:
english
Journal:
BMC Neurology
DOI:
10.1186/s12883-017-0933-z
Date:
December, 2017
File:
PDF, 665 KB
english, 2017