Rett A.: [On an unusual brain atrophy syndrome in hyperammonemia in childhood ]. Wien Med Wochenschr1966;116:723—726.
2.
Hagberg B., Aicardi J., Dias K., Ramos O.: A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett syndrome—Report of 35 cases. Ann Neurol1983;14:471—479.
3.
Harris JC, Wong DF, Wagner HN Jr, et al: Positron emission tomographic study of D2 dopamine receptor binding and CSF biogenic amine metabolites in Rett syndrome. Am J Med Genet1986;24:201—210.
4.
Sirianni N., Naidu S., Pereira J., et al:Rett syndrome: Confirmation of X-linked dominant inheritance, and localization of the gene to Xq28. Am J Hum Genet1998;63(5):1552—1558.
5.
Amir RE, van den Veyver IB, Wan M., et al: Rett syndrome is caused by mutations in X-linked MeCP2, encoding methyl-CpG binding protein 2. Nat Genet1999 ;23:185—188.
