Work

hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes.

Year: 2014

Type: article

Study design: Observational Study

Source: HAL

Authors: 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

Institutions: Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Institut du Cerveau

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: W4299309420

FWCI:

Cites:

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Related to: 10