Fine Mapping of Autistic Disorder to Chromosome 15q11-q13 by Use of Phenotypic Subtypes

Autistic disorder (AutD) is a complex genetic disease. Available evidence suggests that several genes contribute to the underlying genetic risk for the development of AutD. However, both etiologic heterogeneity and genetic heterogeneity confound the discovery of AutD-susceptibility genes. Chromosome...

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Main Authors: Shao, Yujun, Cuccaro, M. L., Hauser, E. R., Raiford, K. L., Menold, M. M., Wolpert, C. M., Ravan, S. A., Elston, L., Decena, K., Donnelly, S. L., Abramson, R. K., Wright, H. H., DeLong, G. R., Gilbert, J. R., Pericak-Vance, M. A.
Formato: Artigo
Idioma:Inglês
Publicado: The American Society of Human Genetics 2003
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Articles
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1180230/
https://ncbi.nlm.nih.gov/pubmed/12567325
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