Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder

Autism spectrum disorder (ASD) is a neurodevelopmental condition that results in behavioral, social and communication impairments. ASD has a substantial genetic component, with 88–95% trait concordance among monozygotic twins. Efforts to elucidate the causes of ASD have uncovered hundreds of suscept...

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Detalles Bibliográficos
Autores principales: Vardarajan, B N, Eran, A, Jung, J-Y, Kunkel, L M, Wall, D P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669925/
https://www.ncbi.nlm.nih.gov/pubmed/23715297
http://dx.doi.org/10.1038/tp.2013.38

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669925/
https://www.ncbi.nlm.nih.gov/pubmed/23715297
http://dx.doi.org/10.1038/tp.2013.38

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