Author:
Bouslam Naima,Bouhouche Ahmed,Benomar Ali,Hanein Sylvain,Klebe Stephan,Azzedine Hamid,Giandomenico Silvia Di,Boland-Augé Anne,Santorelli Filippo M.,Durr Alexandra,Brice Alexis,Yahyaoui Mohamed,Stevanin Giovanni
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference23 articles.
1. Ben Hamida M, Attia-Romdhane N, Hentati F, Triki C (1993) Early onset ataxias in Tunisia. Intrafamilial heterogeneity Adv Neurol 61:105–114
2. Ben Hamida M, Attia-Romdhane N, Triki CH, Oueslati S, Hentati F (1991) (Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich’s disease and P. Marie’s hereditary ataxias) [French]. Rev Neurol (Paris) 147:798–808
3. Caldecott KW (2003) DNA single-strand break repair and spinocerebellar ataxia. Cell 112:7–10
4. Campuzano V, Montermini L, Molto MD, Pianese L, Cossee M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Canizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel J-L, Cocozza S, Koenig M, Pandolfo M (1996) Friedreich’s ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science 271:1423–1427
5. Cottingham RW, Jr. Idury RM, Schaffer AA (1993) Faster sequential genetic linkage computations. Am J Hum Genet 53:252–263
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