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

Publisher： John Wiley & Sons Inc

E-ISSN： 1346-8138|42|8|821-822

ISSN： 0385-2407

Source： THE JOURNAL OF DERMATOLOGY, Vol.42, Iss.8, 2015-08, pp. : 821-822

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