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Association analysis of RTEL1 variants with risk of adult gliomas in a Korean population

Previous studies have identified multiple loci for inherited susceptibility to glioma development, including the regulator of telomere elongation helicase 1 (RTEL1). However, the association between RTEL1 variants and risk of glioma has not been well understood. Therefore, we sought to comprehensive...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:PLoS One
Päätekijät: Namgoong, Suhg, Cheong, Hyun Sub, Kim, Jeong-Hyun, Kim, Lyoung Hyo, Seo, Jung Yeon, Kang, Seok-Gu, Yoon, Seon-Jin, Kim, Se Hoon, Chang, Jong Hee, Shin, Hyoung Doo
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Public Library of Science 2018
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6248978/
https://ncbi.nlm.nih.gov/pubmed/30462709
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0207660
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