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MECP2 gene mutation

Mutation of X chromosome MeCP2 gene results in neurological defects in human females (Rett syndrome) and mice. [Pg.320]

Balmer D, Arredondo J, Samaco RC, LaSaUe JM (2002) MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain. Hum Genet 110 545-552. [Pg.123]

See other pages where MECP2 gene mutation is mentioned: [Pg.373]    [Pg.322]    [Pg.564]    [Pg.464]    [Pg.469]    [Pg.4]    [Pg.117]    [Pg.36]   
See also in sourсe #XX -- [ Pg.30 , Pg.373 ]

See also in sourсe #XX -- [ Pg.373 ]



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MECP2 gene

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