Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis

Candidate gene and genome-wide association study based common risk variant identification is being complemented by whole exome sequencing (WES)/whole genome sequencing based rare variant discovery in elucidation of genetic landscape of schizophrenia (SZ), a common neuropsychiatric disorder. WES find...

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發表在:Schizophr Bull
Main Authors: John, Jibin, Sharma, Aditya, Kukshal, Prachi, Bhatia, Triptish, Nimgaonkar, Vishwajit L, Deshpande, Smita N, Thelma, B K
格式: Artigo
語言:Inglês
出版: Oxford University Press 2019
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6293225/
https://ncbi.nlm.nih.gov/pubmed/29385606
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/schbul/sbx196
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