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hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes

✍ Scribed by Le Ber, Isabelle; Van Bortel, Inge; Nicolas, Gael; Bouya-Ahmed, Kawtar; Camuzat, Agnès; Wallon, David; De Septenville, Anne; Latouche, Morwena; Lattante, Serena; Kabashi, Edor; Jornea, Ludmila; Hannequin, Didier; Brice, Alexis

Book ID: 123466364
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 149 KB
Volume: 35
Category: Article
ISSN: 0197-4580
DOI: 10.1016/j.neurobiolaging.2013.09.016

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