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Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients

Year: 2009

Type: article

Study design: Observational Study

Source: Journal of the Neurological Sciences

DOI: 10.1016/j.jns.2008.12.004

Authors: M. Tazir, L. Ali-Pacha, A. M'Zahem, J.P. Delaunoy, M. Fritsch, S. Nouioua, T. Benhassine, S. Assami, D. Grid, J.M. Vallat, A. Hamri, M. Koenig

Institutions: Hôpital Mustapha Pacha, Centre Hospitalo-Universitaire Dr Benbadis Constantine, Hôpital Civil, Strasbourg, University of Sciences and Technology Houari Boumediene, Genethon (France), Centre Hospitalier Universitaire de Limoges, Centre National de la Recherche Scientifique, Inserm, Institut de génétique et de biologie moléculaire et cellulaire

Language: English

Topic: Genetic Neurodegenerative Diseases

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Institut National de la Santé et de la Recherche Médicale, Ministère de la Santé, Centre National de la Recherche Scientifique

OpenAlex ID: W2095366362

FWCI: 3.042

Cites: 16

Cited by: 64

Related to: 10