Autosomal recessive cerebellar ataxia type 3 due to ANO10 mutations: delineation and genotype-phenotype correlation study.
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N. Drouot | A. Durr | M. Koenig | J. Pouget | H. Scheffer | C. Redin | F. Mochel | H. Kremer | S. Vermeer | E. Kamsteeg | M. Anheim | C. Tranchant | E. Salort-Campana | C. Verschuuren-Bemelmans | J. Muller | M. Mallaret | M. Renaud
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