Genetic copy number variants in sib pairs both affected with schizophrenia

BACKGROUND: Schizophrenia is a complex disorder with involvement of multiple genes. METHODS: In this study, genome-wide screening for DNA copy-number variations (CNVs) was conducted for ten pairs, a total of 20 cases, of affected siblings using oligonucleotide array-based CGH. RESULTS: We found nega...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Lee, Chia-Huei, Liu, Chih-Min, Wen, Chun-Chiang, Chang, Shun-Min, Hwu, Hai-Gwo
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2010
Gaiak:
Research
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2843606/
https://ncbi.nlm.nih.gov/pubmed/20064257
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1423-0127-17-2
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