Recurrent heterozygous missense mutation, p.Gly573Ser, in the TRPV3 gene in an Indian boy with sporadic Olmsted syndrome.

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Published in Br J Dermatol on August 01, 2012

Authors

J E Lai-Cheong1, G Sethuraman, M Ramam, K Stone, M A Simpson, J A McGrath

Author Affiliations

1: St John's Institute of Dermatology, King's College London (Guy's Campus), London SE1 9RT, U.K.

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