What does the nature of the MECP2 mutation tell us about parental origin and recurrence risk in Rett syndrome?

J. Zhang, X. Bao, G. Cao, S. Jiang, X. Zhu, H. Lu, L. Jia, H. Pan, S. Fehr, M. Davis, Helen Leonard, David Ravine, X. Wu

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)
Original languageEnglish
Pages (from-to)526-533
JournalClinical Genetics
Issue number6
Publication statusPublished - 2012

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