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

Salma Ben-Salem, Nara Sobreira, Aisha M. Al-Shamsi, David Valle, Bassam R. Ali, Lihadh Al-Gazali

Research output: Contribution to journalArticle

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

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Qc-SNARE Proteins
Qb-SNARE Proteins
Palmoplantar Keratoderma
Neurocutaneous Syndromes
Founder Effect
Ichthyosis
Newborn Infant
Mutation

ASJC Scopus subject areas

  • Dermatology

Cite this

New Arab family with cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome suggests a possible founder effect for the c.223delG mutation. / Ben-Salem, Salma; Sobreira, Nara; Al-Shamsi, Aisha M.; Valle, David; Ali, Bassam R.; Al-Gazali, Lihadh.

In: Journal of Dermatology, Vol. 42, No. 8, 01.08.2015, p. 821-822.

Research output: Contribution to journalArticle

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AU - Ali, Bassam R.

AU - Al-Gazali, Lihadh

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