Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families

Author:

Benomar Ali,Yahyaoui Mohammed,Meggouh Farid,Bouhouche Ahmed,Boutchich Mohammed,Bouslam Naima,Zaim Abdelhaq,Schmitt Michèle,Belaidi Halima,Ouazzani Reda,Chkili Taı̈b,Koenig Michel

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference13 articles.

1. Mapping of mutation causing Friedreich's ataxia to human chromosome 9;Chamberlain;Nature,1988

2. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion;Campuzano;Science,1996

3. Clinical features and classification of inherited ataxias;Harding,1993

4. Benomar A, Ouhabi H, Zembrag S, et al. les hérédodégnéresences spino-cérébelleuses au Maroc: étude de 225 cas, Ropport du Xème congrès annuel de la panafricaine Neurological Society, Marrakech, Mai 1992.

5. Friedeich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families;Ben Hamida;Neurology,1993

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