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

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

Research output: Contribution to journalLetterpeer-review

10 Citations (Scopus)

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