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TLR2 2258 G>A single nucleotide polymorphism and the risk of congenital infection with human cytomegalovirus
BACKGROUND: Human cytomegalovirus (HCMV) is responsible for the most common intrauterine infections, which may be acquired congenitally from infected pregnant woman to fetus. The research was aimed to estimate the role of three single nucleotide polymorphisms (SNPs) located in TLR2 gene, and the com...
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| Pubblicato in: | Virol J |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5260049/ https://ncbi.nlm.nih.gov/pubmed/28118851 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12985-016-0679-z |
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