Work

Variabilité phénotypique de deux familles AR CMT avec une mutation du gène GDAP1

Year: 2015

Type: article

Study design: Case Report

Source: Revue Neurologique

DOI: 10.1016/j.neurol.2015.01.323

Authors: Mounia Bellatache, Sonia Nouioua, Corine Magdelaine, Salima Assami, Jean-Michel Vallat, Meriem Tazir

Institutions: Hôpital Mustapha Pacha, Centre Hospitalier Universitaire de Limoges

Language: French

Topic: Hereditary Neurological Disorders

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W1986005207

FWCI:

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