Variant Rett syndrome in a girl with a pericentric X-chromosome inversion leading to epigenetic changes and overexpression of the MECP2 gene

J.P. Vieira, F. Lopes, A. Silva-Fernandes, M.V. Sousa, S. Moura, S. Sousa, B.M. Costa, M. Barbosa, B. Ylstra, T. Temudo, T. Lourenco, P. Maciel

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)82-87
JournalInternational Journal of Developmental Neuroscience
Publication statusPublished - 2015

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