De novo occurrence of the 730insG recurrent mutation in an Italian family with the ichthyotic variant of Vohwinkel syndrome, loricrin keratoderma [1]

B. Drera, G. Tadini, F. Balbo, L. Marchese, S. Barlati, Marina Colombi

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)85-88
Number of pages4
JournalClinical Genetics
Volume73
Issue number1
DOIs
Publication statusPublished - Jan 2008

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this