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Human Molecular Genetics, Vol. 9, Iss. 7, 2000-04 ,pp. : 1119-1129

Oxford University Press

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A rare male patient with classic Rett syndrome caused by MeCP2_e1 mutation

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American Journal Of Medical Genetics Part A, Vol. 176, Iss. 3, 2018-03 ,pp. : 699-702

John Wiley & Sons Inc

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MECP2 mutations account for most cases of typical forms of Rett syndrome

By Bienvenu Thierry   Carrié Alain   de Nicolas  

Human Molecular Genetics, Vol. 9, Iss. 9, 2000-05 ,pp. : 1377-1384

Oxford University Press

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Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients

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Human Molecular Genetics, Vol. 9, Iss. 9, 2000-05 ,pp. : 1369-1375

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MeCP2 in neurons: closing in on the causes of Rett Syndrome

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