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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 |
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| Authors: | Salma Ben‐Salem Sobreira Nara Aisha M. Al‐Shamsi David Valle Bassam R. Ali Lihadh Al‐Gazali |
| Affiliation: | 1. Department of Pathology, College of Medicine and Heath Sciences, United Arab Emirates University, Al‐Ain, United Arab Emirates;2. Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA;3. Department of Pediatrics, Tawam Hospital, Al‐Ain, United Arab Emirates;4. Department of Pediatrics, College of Medicine and Heath Sciences, United Arab Emirates University, Al‐Ain, United Arab Emirates |
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