Detection of mutations in MECP2 gene in Egyptian patients with Rett syndrome
Wessam El-Saeed Mohamed Sharaf El-Din;
Abstract
Rett syndrome (RTT) is a severe progressive
neurodevelopmental disorder that affects mainly females
representing one of the most common causes of mental
retardation in girls with a prevalence estimated to be 1 in each
10,000-15,000 female births.
The pres
neurodevelopmental disorder that affects mainly females
representing one of the most common causes of mental
retardation in girls with a prevalence estimated to be 1 in each
10,000-15,000 female births.
The pres
Other data
| Title | Detection of mutations in MECP2 gene in Egyptian patients with Rett syndrome | Other Titles | تحديد الطفرات في جين 2 MECP في المرضى المصريين المصابين بمتلازمة رت | Authors | Wessam El-Saeed Mohamed Sharaf El-Din | Keywords | Detection of mutations in MECP2 gene in Egyptian patients with Rett syndrome | Issue Date | 2011 | Description | Rett syndrome (RTT) is a severe progressive neurodevelopmental disorder that affects mainly females representing one of the most common causes of mental retardation in girls with a prevalence estimated to be 1 in each 10,000-15,000 female births. The pres |
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