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New Arab family with cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome suggests a possible founder effect for the c.223delG mutation
Author(s) -
BenSalem Salma,
Nara Sobreira,
AlShamsi Aisha M.,
Valle David,
Ali Bassam R.,
AlGazali Lihadh
Publication year - 2015
Publication title -
the journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 65
eISSN - 1346-8138
pISSN - 0385-2407
DOI - 10.1111/1346-8138.12917
Subject(s) - medicine , matriculation , family medicine , traditional medicine , medical education
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