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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.
Authors
BALBO F
BARLATI S
+4 more
COLOMBI M
DRERA B
MARCHESE L
TADINI G
Publication date
1 January 2008
Publisher
'Wiley'
Doi
Abstract
Abstract is not available.
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Archivio istituzionale della ricerca - Università di Brescia
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oai:iris.unibs.it:11379/28518
Last time updated on 12/11/2016