References Regarding Rett Syndrome:
Amir RE, Fang P, Yu Z, Glaze D, Percy AK, Zoghbi HY, Roa BB, Van den Veyver, IB. Mutations in exon 1 of MECP2 are a rare cause of Rett Syndrome. J Medical Genet, on-line publication, 2004.
Neul JL, Maricich SM, Islam M, Barrish J, Smith EO, Bottiglieri T, Hyland K, Humphreys P, Percy A, Glaze D. Spinal fluid 5-methyltetrahydrofolate levels are normal in Rett Syndrome. Neurology: in press, 2005.
Percy AK. Rett Syndrome: Clinical and Molecular Update. Current Opinion in Pediatrics 16:670-677, 2004.