Work

Autosomal dominant cerebellar ataxia type I in Morocco: presence of the SCA1 and SCA3/MJD mutations

Year: 1996

Type: article

Study design: Observational Study

Source: European Journal of Neurology

DOI: 10.1111/j.1468-1331.1996.tb00231.x

Authors: A. Benomar, F. Meggouh, O. Didierjean, N. Kissani, A. Dürr, A. Sefiani, T. Chkili, Y. Agid, M. Yahyaoui, A. Brice

Institutions: Institut National d'Hygiène du Maroc, Inserm, Physiopathologie des Comportements

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

Funder: Institut National de la Santé et de la Recherche Médicale

OpenAlex ID: W2122504852

FWCI:

Cites: 10

Cited by: 2

Related to: 10