UBQLN2 mutations are rare in French and French–Canadian...

UBQLN2 mutations are rare in French and French–Canadian amyotrophic lateral sclerosis

Hussein Daoud, Hamid Suhail, Anna Szuto, William Camu, Francois Salachas, Vincent Meininger, Jean-Pierre Bouchard, Nicolas Dupré, Patrick A. Dion, Guy A. Rouleau
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Volume:
33
Year:
2012
Language:
english
DOI:
10.1016/j.neurobiolaging.2012.03.015
File:
PDF, 876 KB
english, 2012
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