Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia

BACKGROUND: Autosomal recessive cerebellar ataxias (ARCA) are a complex group of neurodegenerative disorders with great genetic and phenotypic heterogeneity, over 30 genes/loci have been associated with more than 20 different clinical forms of ARCA. Genetic heterogeneity combined with highly variabl...

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Detalles Bibliográficos
Autores principales: Hamza, Wahiba, Ali Pacha, Lamia, Hamadouche, Tarik, Muller, Jean, Drouot, Nathalie, Ferrat, Farida, Makri, Samira, Chaouch, Malika, Tazir, Meriem, Koenig, Michel, Benhassine, Traki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630839/
https://www.ncbi.nlm.nih.gov/pubmed/26068213
http://dx.doi.org/10.1186/s12881-015-0180-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630839/
https://www.ncbi.nlm.nih.gov/pubmed/26068213
http://dx.doi.org/10.1186/s12881-015-0180-3

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