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John Wiley & Sons Inc

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A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family

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John Wiley & Sons Inc

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Comparative mapping of oculocutaneous albinism type II (OCA2), transient receptor potential cation channel, subfamily M member 1 (TRPM1) and two equine microsatellites, ASB08 and 1CA43, among four equid species by fluorescence in situ hybridization

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The Pink‐Eyed Dilution Gene and the Molecular Pathogenesis of Tyrosinase‐Positive Albinism (OCA2)

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Two novel missense mutations of STS gene underlie X‐linked recessive ichthyosis: understanding of the mutational and structural spectrum

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