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M - 10 Mutations du gène NIPA1 (SPG6) : une cause rare de paraparésie spastique héréditaire en Europe

Year: 2007

Type: article

Study design: Observational Study

Source: Revue Neurologique

DOI: 10.1016/s0035-3787(07)90706-7

Authors: S. Klebe, A. Lacour, A. Durr, T. Stojkovic, C. Depienne, S. Forlani, S. Poca-Guyon, I. Vuillaume, B. Sablonniere, P. Vermersch, A. Brice, G. Stevanin

Institutions: Inserm, Pitié-Salpêtrière Hospital, Hôpital Roger Salengro

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: W1978730413

FWCI:

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Related to: 10