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Epilepsy in Rett syndrome: Association between phenotype and genotype, and implications for practice

  • Published:2011-10 Issue:8 Volume:20 Page:646-649
  • ISSN:1059-1311
  • Container-title:Seizure
  • language:en
  • Short-container-title:Seizure

Author:

Cardoza Basil,Clarke Angus,Wilcox Jodie,Gibbon Frances,Smith Phil E.M.,Archer Hayley,Hryniewiecka-Jaworska Anna,Kerr Mike

Funder

Rett UK

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology,General Medicine

Reference30 articles.

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein;Amir;Nat Genet,1999

2. Survey of adolescents with severe intellectual handicap;Asthana;Arch Dis Child,1990

3. A study of Rett syndrome in the GDR;Kultz;Brain Dev,1990

4. Early clinical signs in the Rett disorder;Kerr;Neuropaediatrics,1995

5. Rett syndrome: a comprehensive review of the literature;Perry;Am J Ment Retard,1991
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