Correlation between clinical features and MECP2 gene mutations in patients with rett syndrome
By: Mujahid, Hisham; Hindawi, Aminah; Muhammadi, Muhammad. Egyptian Pediatric Association Gazette. Vol. 63, no. 1 (Mar. 2015), pp.25-31, 7 p.
Subjects: Egypt; Genetic aspects; Mental deficiency; Patients