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Common and rare exonic MUC5B variants associated with type 2 diabetes in Han Chinese

Genome-wide association studies have identified over one hundred common genetic risk variants associated with type 2 diabetes (T2D). However, most of the heritability of T2D has not been accounted for. In this study, we investigated the contribution of rare and common variants to T2D susceptibility...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:PLoS One
Päätekijät: Chen, Guanjie, Zhang, Zhenjian, Adebamowo, Sally N., Liu, Guozheng, Adeyemo, Adebowale, Zhou, Yanxun, Doumatey, Ayo P., Wang, Chuntao, Zhou, Jie, Yan, Wenqiang, Shriner, Daniel, Tekola-Ayele, Fasil, Bentley, Amy R., Jiang, Congqing, Rotimi, Charles N.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Public Library of Science 2017
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5367689/
https://ncbi.nlm.nih.gov/pubmed/28346466
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0173784
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