piebaldism/proline

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[Identification of a novel KIT mutation in a Chinese family affected with piebaldism].

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Prijava / prijava

OBJECTIVE To identify the pathogenic mutation underlying piebaldism in a Chinese family. METHODS A three-generation family showing an autosomal dominant transmission of piebaldism was recruited. Potential mutations of the KIT and SNAI2 genes were detected by PCR-amplification of the exons and

A novel mutation of the KIT gene in a Chinese family with piebaldism.

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BACKGROUND Human piebaldism is a rare autosomal dominant condition characterized by congenital white forelock and depigmented patches of skin, typically on the forehead, anterior trunk and extremities. Mutations in the KIT gene have been proposed to be responsible for the underlying changes in this

Biochemical and functional characterization of Rab27a mutations occurring in Griscelli syndrome patients.

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Prijava / prijava

Rab27a is a member of the Rab family of small GTPase proteins, and thus far is the first member to be associated with a human disease (ie, the Griscelli syndrome type 2). Mutations in the Rab27a gene cause pigment as well as cytotoxic granule transport defects, accounting for the partial albinism

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Herbal & Natural Medicine

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