Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein.
Watson, Pamela; Black, Graeme; Ramsden, Simon; Barrow, Margaret; Super, Maurice; Kerr, Bronwyn; Clayton-Smith, Jill; Journal of Medical Genetics, 2001, vol. 38, issue 4, p 224, ISSN 00222593. ISBN 14686244.

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