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Publications by A Benomar
The First De Novo Mutation of the Connexin 32 Gene Associated With X Linked Charcot-Marie-Tooth Disease.
Journal of Medical Genetics
Genetics
Multiple Origins of the Spinocerebellar Ataxia 7 (SCA7) Mutation Revealed by Linkage Disequilibrium Studies With Closely Flanking Markers, Including an Intragenic Polymorphism (G3145tg/A3145tg)
European Journal of Human Genetics
Genetics