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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 LacombleVolume:
33
Year:
2012
DOI:
10.1016/j.neurobiolaging.2011.11.010
File:
PDF, 345 KB
2012