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Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder

BACKGROUND: Obsessive-compulsive disorder (OCD) is a clinically and etiologically heterogeneous syndrome. The high frequency of obsessive-compulsive symptoms reported in subjects with the 22q11.2 deletion syndrome (DiGeorge/velocardiofacial syndrome) or Prader-Willi syndrome (15q11-13 deletion of th...

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Detalhes bibliográficos
Main Authors: Delorme, Richard, Moreno-De-Luca, Daniel, Gennetier, Aurélie, Maier, Wolfgang, Chaste, Pauline, Mössner, Rainald, Grabe, Hans Jörgen, Ruhrmann, Stephan, Falkai, Peter, Mouren, Marie-Christine, Leboyer, Marion, Wagner, Michael, Betancur, Catalina
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2010
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2909937/
https://ncbi.nlm.nih.gov/pubmed/20565924
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-11-100
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