A novel mutation in the kinase domain of KIT in an Indian family with a mild piebaldism phenotype

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2010-09-01

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Therapeutic siRNAs for dominant genetic skin disorders including pachyonychia congenita
A novel mutation in the kinase domain of KIT in an Indian family with a mild piebaldism phenotype
A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita

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