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A Novel Mutation In Frabin (FGD4) Causing A Mild Phenotype Of CMT4H In An Indian Patient
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Title: A novel mutation in frabin ( fgd4) causing a mild phenotype of cmt4h inA novel mutation in frabin ( fgd4) causing a mild phenotype of cmt4h in.
Title: A novel mutation in frabin ( fgd4) causing a mild phenotype of cmt4h inA novel mutation in frabin ( fgd4) causing a mild phenotype of cmt4h in.
Title: A novel frabin (fgd4) nonsense mutation p.r275x associated withA novel frabin (fgd4) nonsense mutation p.r275x associated with.
