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The Distribution of Disease-Associated Copy Number Variants Across Distinct Disorders of Cognitive Development

OBJECTIVE: The purpose of the present study is to discover the extent to which distinct DSM disorders share large, highly recurrent copy number variants (CNVs) as susceptibility factors. We also seek to identify gene mechanisms common to groups of diagnoses and/or specific to a given diagnosis based...

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Autori principali: Pescosolido, Matthew F., Gamsiz, Ece D., Nagpal, Shailender, Morrow, Eric M.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2013
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3774163/
https://ncbi.nlm.nih.gov/pubmed/23582872
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaac.2013.01.003
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