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[DOI] [PMC free article] [PubMed] [Google Scholar] 50.Zheng W., Zhang Q.E., Cai D.B., Yang X.H., Qiu Y., Ungvari G., Ng C., Berk M., Ning Y.P., Xiang Y.T
Biomedicines 10:2907
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As a severe X-linked neurodevelopmental disorder, RTT predominantly affects females, with the majority of cases resulting from MECP2 mutations both within and outside the methyl-CpG binding domain (MBD) (98)
