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Identification of rare and common variants in BNIP3L: a schizophrenia susceptibility gene
BACKGROUND: Schizophrenia is a chronic and severe mental disorder, and it has been predicted to be highly polygenic. Common SNPs located in or near BNIP3L were found to be genome-wide significantly associated with schizophrenia in recent genome-wide association studies. The purpose of our study is t...
Tallennettuna:
| Julkaisussa: | Hum Genomics |
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| Päätekijät: | , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7212671/ https://ncbi.nlm.nih.gov/pubmed/32393399 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40246-020-00266-4 |
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