The Angelman, Rett and Prader-Willi Syndromes Consortium Child looking up

University of Alabama at Birmingham - Birmingham, Alabama

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Contact Information:

Alan Percy, M.D.
Pediatric Neurology
University of Alabama at Birmingham
E-mail: apercy@peds.uab.edu

Jane Lane
E-mail: jlane@uab.edu

Recommended Links:

Current Clinical Studies:

5201: Rett Syndrome Natural History Study

List of Publications:

1. 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.

2. 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.

3. Percy AK. Rett Syndrome: Clinical and Molecular Update. Current Opinion in Pediatrics 16:670-677, 2004.

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