No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathy

✍ Scribed by Seelen, Meinie; Visser, Anne E.; Overste, Daniel J.; Kim, Hong J.; Palud, A.; Wong, Tsz H.; van Swieten, John C.; Scheltens, Philip; Voermans, Nicol C.; Baas, Frank; de Jong, J.M.B.V.; van der Kooi, Anneke J.; de Visser, Marianne; Veldink, Jan H.; Taylor, J. Paul; Van Es, Michael A.; van den Berg, Leonard H.

• Book ID: 123594738
• Publisher: Elsevier Science
• Year: 2014
• Tongue: English
• Weight: 177 KB
• Volume: 35
• Category: Article
• ISSN: 0197-4580
• DOI: 10.1016/j.neurobiolaging.2014.01.152