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

Source: Clinical Genetics, Volume 73, Number 1, January 2008 , pp. 85-88(4)

Publisher: Blackwell Publishing

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Document Type: Research article

DOI: 10.1111/j.1399-0004.2007.00914.x

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