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A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure
Perandones, Claudia, Pellene, Luis Alejandro, Micheli, FedercioVolume:
29
Language:
english
Journal:
Movement Disorders
DOI:
10.1002/mds.25738
Date:
January, 2014
File:
PDF, 110 KB
english, 2014