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

✍ Scribed by Hussein Daoud; Hamid Suhail; Anna Szuto; William Camu; Francois Salachas; Vincent Meininger; Jean-Pierre Bouchard; Nicolas Dupré; Patrick A. Dion; Guy A. Rouleau

Book ID: 116781921
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 876 KB
Volume: 33
Category: Article
ISSN: 0197-4580
DOI: 10.1016/j.neurobiolaging.2012.03.015

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