Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein
Watson, P.; Black, G.; Ramsden, S.; Barrow, M.; Super, M.; Kerr, B.; Clayton-Smith, J.; Journal of Medical Genetics (JMG), 2001, vol. 38, issue 4, p 224, ISSN 00222593. ISBN 14686244.

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