Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis

✍ Scribed by Stéphanie Millecamps; Philippe Corcia; Cécile Cazeneuve; Séverine Boillée; Danielle Seilhean; Véronique Danel-Brunaud; Nadia Vandenberghe; Pierre-François Pradat; Nadine Le Forestier; Lucette Lacomblez; Gaëlle Bruneteau; William Camu; Alexis Brice; Vincent Meininger; Eric LeGuern; François Salachas

• Book ID: 116781786
• Publisher: Elsevier Science
• Year: 2012
• Tongue: English
• Weight: 345 KB
• Volume: 33
• Category: Article
• ISSN: 0197-4580
• DOI: 10.1016/j.neurobiolaging.2011.11.010