Zobrazeno 1 - 1
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pro vyhledávání: '"Wessam E. Sharaf El-Din"'
Publikováno v:
Egyptian Journal of Medical Human Genetics; Vol 13, No 1 (2012); 19-27
Rett syndrome (RTT) is a progressive neurodevelopmental disorder that affects mainly females comprising one of the most common causes of mental retardation in females. Mutations in the X-linked MECP2 gene have been identified to be the major cause fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58f8b821cca8ddee76c1386cff7359d4
https://doi.org/10.1016/j.ejmhg.2011.11.004
https://doi.org/10.1016/j.ejmhg.2011.11.004
