ロード中...
Slc22a5 haploinsufficiency does not aggravate the phenotype of the long-chain acyl-CoA dehydrogenase KO mouse
Secondary carnitine deficiency is commonly observed in inherited metabolic diseases characterized by the accumulation of acylcarnitines such as mitochondrial fatty acid oxidation (FAO) disorders. It is currently unclear if carnitine deficiency and/or acylcarnitine accumulation play a role in the pat...
保存先:
| 出版年: | J Inherit Metab Dis |
|---|---|
| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2019
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7205564/ https://ncbi.nlm.nih.gov/pubmed/31845336 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jimd.12204 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|