3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances

BACKGROUND: In contrast to other autism spectrum disorders, chromosome abnormalities are rare in Asperger syndrome (AS) or high-functioning autism. Consequently, AS was occasionally subjected to classical positional cloning. Here, we report on a case of AS associated with a deletion of the short arm...

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Detalles Bibliográficos
Autores principales: Iourov, Ivan Y., Vorsanova, Svetlana G., Voinova, Victoria Y., Yurov, Yuri B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628252/
https://www.ncbi.nlm.nih.gov/pubmed/26523151
http://dx.doi.org/10.1186/s13039-015-0185-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628252/
https://www.ncbi.nlm.nih.gov/pubmed/26523151
http://dx.doi.org/10.1186/s13039-015-0185-9

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