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 journalArticle

7 Citations (Scopus)
Original languageEnglish
Pages (from-to)526-533
JournalClinical Genetics
Volume82
Issue number6
DOIs
Publication statusPublished - 2012

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