New Arab family with cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome suggests a possible founder effect for the c.223delG mutation

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
Pages (from-to)821-822
Number of pages2
JournalJournal of Dermatology
Volume42
Issue number8
DOIs
Publication statusPublished - Aug 1 2015

ASJC Scopus subject areas

  • Dermatology

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