ArticleInternational journal of molecular and cellular medicine2019

Whole Exome Sequencing Revealed a Novel GJB1 Pathogenic Variant and a Rare BSCL2 Mutation in Two Iranian Large Pedigrees with Multiple Affected Cases of Charcot-Marie-Tooth.

Neda Mohsenpour et al.PubMed ↗Full text ↗Publisher ↗

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