The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders

Over the last fifteen years it has become established that 22q11.2 deletion syndrome (22q11DS) is a true genetic risk factor for schizophrenia. Carriers of deletions in chromosome 22q11.2 develop schizophrenia at rate of 25–30% and such deletions account for as many as 1–2% of cases of sporadic schi...

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Main Authors: Drew, Liam J., Crabtree, Gregg W., Markx, Sander, Stark, Kimberly L., Chaverneff, Florence, Xu, Bin, Mukai, Jun, Fenelon, Karine, Hsu, Pei-Ken, Gogos, Joseph A., Karayiorgou, Maria
Format: Artigo
Language:Inglês
Published: 2010
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3074020/
https://ncbi.nlm.nih.gov/pubmed/20920576
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijdevneu.2010.09.007
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