Genome-wide copy number variation analysis of hepatitis B infection in a Japanese population

Genome-wide association studies have been performed to identify common genetic variants associated with hepatitis B (HB). However, little is known about copy number variations (CNVs) in HB. In this study, we performed a genome-wide CNV analysis between 1830 healthy controls and 1031 patients with HB...

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Detalhes bibliográficos
Publicado no:Hum Genome Var
Main Authors: Kikuchi, Masataka, Kobayashi, Kaori, Nishida, Nao, Sawai, Hiromi, Sugiyama, Masaya, Mizokami, Masashi, Tokunaga, Katsushi, Nakaya, Akihiro
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2021
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8187437/
https://ncbi.nlm.nih.gov/pubmed/34103483
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41439-021-00154-w
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