2003•Pediatric NeurologyRequires access

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

Regina M. Carney, Chantelle M. Wolpert, Sarah A. Ravan, Mona D. Shahbazian, Allison E. Ashley‐Koch, Michael L. Cuccaro, Jeffery M. Vance, Margaret A. Pericak‐Vance

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Key concepts: MECP2, Rett syndrome, Neurodevelopmental disorder, Developmental disorder, Autism, Autism spectrum disorder, Phenotype, Genetics

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Identification of MeCP2 mutations in a series of females with autistic disorder — Research Paper | ScholarLens