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Lack of global epigenetic methylation defects in CBS deficient mice
Cystathionine β-synthase (CBS) deficiency is a recessive inborn error of metabolism in which patients have extremely elevated plasma total homocysteine and have clinical manifestations in the vascular, visual, skeletal, and nervous systems. Homocysteine is an intermediary metabolite produced from th...
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| Publicado no: | J Inherit Metab Dis |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5300059/ https://ncbi.nlm.nih.gov/pubmed/27444757 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10545-016-9958-5 |
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