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Article Dans Une Revue Muscle & nerve. Supplement. Année : 2017

γ-sarcoglycan and dystrophin mutation spectrum in an Algerian cohort

Résumé

We report the genetic analysis of a large series of 76 Algerian patients from 65 unrelated families who presented with early onset severe muscular dystrophy and a clinical phenotype resembling limb-girdle muscular dystrophy type 2C.
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Dates et versions

hal-02333075 , version 1 (25-10-2019)

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Evelyne Gicquel, Natacha Maizonnier, Steven Foltz, William Martin, Nathalie Bourg, et al.. γ-sarcoglycan and dystrophin mutation spectrum in an Algerian cohort. Muscle & nerve. Supplement., 2017, 56 (1), pp.129-135. ⟨10.1002/mus.25443⟩. ⟨hal-02333075⟩
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