Mutations in UBQLN2 are rare in French amyotrophic lateral...

Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis

Stéphanie Millecamps, Philippe Corcia, Cécile Cazeneuve, Séverine Boillée, Danielle Seilhean, Véronique Danel-Brunaud, Nadia Vandenberghe, Pierre-François Pradat, Nadine Le Forestier, Lucette Lacomble
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Volume:
33
Year:
2012
DOI:
10.1016/j.neurobiolaging.2011.11.010
File:
PDF, 345 KB
2012
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