Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia-Reference-Cited by-同舟云学术

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

Published:2015-06-12 Issue:1 Volume:16 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Hamza Wahiba,Ali Pacha Lamia,Hamadouche Tarik,Muller Jean,Drouot Nathalie,Ferrat Farida,Makri Samira,Chaouch Malika,Tazir Meriem,Koenig Michel,Benhassine Traki

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/article/10.1186/s12881-015-0180-3/fulltext.html

Reference65 articles.

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2. Fogel BL, Perlman S. Clinical features and molecular genetics of autosomal recessive cerebellar ataxias. Lancet Neurol. 2007;6(3):245–57.

3. Harding AE. Classification of the hereditary ataxias and paraplegias. Lancet. 1983;1(8334):1151–5.

4. Embiruçu EK, Martyn ML, Schlesinger D, Kok F. Autosomal recessive ataxias: 20 types, and counting. Arq Neuropsiquiatr. 2009;67(4):1143–56.

5. Vermeer S, van de Warrenburg BP, Willemsen MA, Cluitmans M, Scheffer H, Kremer BP, et al. Autosomal recessive cerebellar ataxias: the current state of affairs. J Med Genet. 2011;48(10):651–9.

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