New Arab family with cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome suggests a possible founder effect for the c.223delG mutation
Ben-Salem, Salma, Nara, Sobreira, Al-Shamsi, Aisha M., Valle, David, Ali, Bassam R., Al-Gazali, LihadhVolume:
42
Language:
english
Journal:
The Journal of Dermatology
DOI:
10.1111/1346-8138.12917
Date:
August, 2015
File:
PDF, 99 KB
english, 2015