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The Genetics of Clinical Liver Diseases: Insight into the TM6SF2 E167K Variant
The transmembrane 6 superfamily member 2 (TM6SF2) gene E167K variant (rs58542926) was identified by exome-wide association study as a nonsynonymous single nucleotide polymorphism associated with nonalcoholic fatty liver disease. The TM6SF2 E167K variant features a C-to-T substitution at nucleotide 4...
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| Publicado no: | J Clin Transl Hepatol |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
XIA & HE Publishing Inc.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6160302/ https://ncbi.nlm.nih.gov/pubmed/30271746 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14218/JCTH.2018.00022 |
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