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Genetic and Genomic Systems to Study Methylmalonic Acidemia
Methylmalonic acidemia (MMAemia) is the biochemical hallmark of a group of genetic metabolic disorders that share a common defect in the ability to convert methylmalonyl-CoA into succinyl-CoA. This disorder is due to either a mutant methylmalonyl-CoA mutase apoenzyme or impaired synthesis of adenosy...
Tallennettuna:
| Päätekijät: | , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2005
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2657357/ https://ncbi.nlm.nih.gov/pubmed/16182581 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2005.07.020 |
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