Work

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

Year: 2013

Type: article

Study design: Observational Study

Source: Neurobiology of Aging

DOI: 10.1016/j.neurobiolaging.2013.09.016

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

Institutions: Centre National de la Recherche Scientifique, Inserm, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Institut du Cerveau, Université Pierre-et-Marie-Curie, Hôpital Charles-Nicolle, Normandie Université, Institute for Research and Innovation in Biomedicine, Université de Rouen Normandie

Language: English

Topic: Amyotrophic Lateral Sclerosis Research

Subfield: Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2047562820

FWCI: 4.867

Cites: 8

Cited by: 65

Related to: 10