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Identification of MeCP2 mutations in a series of females with autistic disorder

✍ Scribed by Regina M. Carney; Chantelle M. Wolpert; Sarah A. Ravan; Mona Shahbazian; Allison Ashley-Koch; Michael L. Cuccaro; Jeffery M. Vance; Margaret A. Pericak-Vance


Book ID
117591180
Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
227 KB
Volume
28
Category
Article
ISSN
0887-8994

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## Abstract Rett syndrome (RS) is one of the best human models to study movement disorders. Patients evolve from a hyperkinetic to a hypokinetic state, and a large series of abnormal movements may be observed along their lives such as stereotypies, tremor, chorea, myoclonus, ataxia, dystonia, and r