A novel INDEL mutation in the EDA gene resulting in a distinct X-linked hypohidrotic ectodermal dysplasia phenotype in an Italian family

M. Callea, P. Nieminen, C. E. Willoughby, G. Clarich, I. Yavuz, Agatino Vinciguerra, M. Di Stazio, S. Giglio, I. Sani, M. Maglione, S. Pensiero, G. Tadini, E. Bellacchio

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)341-343
Number of pages3
JournalJournal of the European Academy of Dermatology and Venereology
Volume30
Issue number2
DOIs
Publication statusPublished - Feb 1 2016

ASJC Scopus subject areas

  • Dermatology
  • Infectious Diseases

Cite this