SCA13 : une nouvelle cause d’ataxie myoclonique autosomique...

SCA13 : une nouvelle cause d’ataxie myoclonique autosomique dominante non progressive

Montaut, Solveig, Apartis, Emmanuelle, Ewenczyk, Claire, Chanson, Jean-Baptiste, Koenig, Michel, Tranchant, Christine, Anheim, Mathieu
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Volume:
172
Language:
french
Journal:
Revue Neurologique
DOI:
10.1016/j.neurol.2016.01.287
Date:
April, 2016
File:
PDF, 52 KB
french, 2016
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