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Mental retardation progressive spasticity
Review Articles from PubMed
Editorials from PubMed
Research Articles from PubMed
Heterozygous mutations in the X-linked MECP2 gene cause Rett syndrome, a severe neurodevelopmental disorder of young females. Only one male presenting an MECP2 mutation has been reported; he survived only to age 1 year, suggesting that mutations in MECP2 are male lethal. Here we report ...