Identification of the functional variant driving ORMDL3 and GSDMB expression in human chromosome 17q12-21 in primary biliary cholangitis

Numerous genome-wide association studies (GWAS) have been performed to identify susceptibility genes to various human complex diseases. However, in many cases, neither a functional variant nor a disease susceptibility gene have been clarified. Here, we show an efficient approach for identification o...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Sci Rep
Päätekijät: Hitomi, Yuki, Kojima, Kaname, Kawashima, Minae, Kawai, Yosuke, Nishida, Nao, Aiba, Yoshihiro, Yasunami, Michio, Nagasaki, Masao, Nakamura, Minoru, Tokunaga, Katsushi
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group UK 2017
Aiheet:
Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5460198/
https://ncbi.nlm.nih.gov/pubmed/28588209
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-03067-3
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