Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease

Hirschsprung disease (HSCR) is the most common cause of neonatal intestinal obstruction. It is characterized by the absence of ganglia in the nerve plexuses of the lower gastrointestinal tract. So far, three common disease-susceptibility variants at the RET, SEMA3 and NRG1 loci have been detected th...

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書誌詳細
出版年:Hum Mol Genet
主要な著者: Tang, Clara Sze-man, Gui, Hongsheng, Kapoor, Ashish, Kim, Jeong-Hyun, Luzón-Toro, Berta, Pelet, Anna, Burzynski, Grzegorz, Lantieri, Francesca, So, Man-ting, Berrios, Courtney, Shin, Hyoung Doo, Fernández, Raquel M., Le, Thuy-Linh, Verheij, Joke B.G.M., Matera, Ivana, Cherny, Stacey S., Nandakumar, Priyanka, Cheong, Hyun Sub, Antiñolo, Guillermo, Amiel, Jeanne, Seo, Jeong-Meen, Kim, Dae-Yeon, Oh, Jung-Tak, Lyonnet, Stanislas, Borrego, Salud, Ceccherini, Isabella, Hofstra, Robert M.W., Chakravarti, Aravinda, Kim, Hyun-Young, Sham, Pak Chung, Tam, Paul K.H., Garcia-Barceló, Maria-Mercè
フォーマット: Artigo
言語:Inglês
出版事項: Oxford University Press 2016
主題:
Association Studies Articles
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6078638/
https://ncbi.nlm.nih.gov/pubmed/27702942
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw333
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