Work

CHMP2B mutations are rare in French families with frontotemporal lobar degeneration

Year: 2010

Type: article

Study design: Observational Study

Source: Journal of Neurology

DOI: 10.1007/s00415-010-5655-8

Authors: Mustapha Ghanim, Léna Guillot-Noel, Florence Pasquier, Ludmila Jornea, Vincent Deramecourt, Bruno Dubois, Isabelle Ber, Alexis Brice

Institutions: Inserm, Université de Lille, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Université Pierre-et-Marie-Curie

Language: English

Topic: Amyotrophic Lateral Sclerosis Research

Subfield: Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Agence Nationale de la Recherche

OpenAlex ID: W2055108144

FWCI: 2.473

Cites: 22

Cited by: 28

Related to: 10