A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R

BACKGROUND: Autism is a pervasive developmental disorder characterized by a triad of deficits: qualitative impairments in social interactions, communication deficits, and repetitive and stereotyped patterns of behavior. Although autism is etiologically heterogeneous, family and twin studies have est...

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Detalles Bibliográficos
Autores principales: Ramanathan, Subhadra, Woodroffe, Abigail, Flodman, Pamela L, Mays, Lee Z, Hanouni, Mona, Modahl, Charlotte B, Steinberg-Epstein, Robin, Bocian, Maureen E, Spence, M Anne, Smith, Moyra
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC411038/
https://www.ncbi.nlm.nih.gov/pubmed/15090072
http://dx.doi.org/10.1186/1471-2350-5-10

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC411038/
https://www.ncbi.nlm.nih.gov/pubmed/15090072
http://dx.doi.org/10.1186/1471-2350-5-10

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