hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes
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Published:2014-04
Issue:4
Volume:35
Page:934.e5-934.e6
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ISSN:0197-4580
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Container-title:Neurobiology of Aging
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language:en
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Short-container-title:Neurobiology of Aging
Author:
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
Funder
Investissements d'avenir France Alzheimer Association Neuromics FP7 Programme Hospitalier de Recherche Clinique
Subject
Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience
Reference7 articles.
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