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De novo occurrence of the 730insG recurrent mutation in an Italian family with the ichthyotic variant of Vohwinkel syndrome, loricrin keratoderma.

By DRERA B, TADINI G, BALBO F, MARCHESE L, BARLATI S and COLOMBI M
Topics: Vohwinkel syndrome, Loricrin, Ichtyosis
Publisher: 'Wiley'
Year: 2008
DOI identifier: 10.1111/j.1399-0004.2007.00914.x
OAI identifier: oai:iris.unibs.it:11379/28518
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