A 15q13.3 microdeletion segregating with autism

Autism and mental retardation (MR) show high rates of comorbidity and potentially share genetic risk factors. In this study, a rare ∼2 Mb microdeletion involving chromosome band 15q13.3 was detected in a multiplex autism family. This genomic loss lies between distal break points of the Prader–Willi/...

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Detalhes bibliográficos
Main Authors: Pagnamenta, Alistair T, Wing, Kirsty, Akha, Elham Sadighi, Knight, Samantha JL, Bölte, Sven, Schmötzer, Gabriele, Duketis, Eftichia, Poustka, Fritz, Klauck, Sabine M, Poustka, Annemarie, Ragoussis, Jiannis, Bailey, Anthony J, Monaco, Anthony P
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2009
Assuntos:
Short Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2986268/
https://ncbi.nlm.nih.gov/pubmed/19050728
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2008.228
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