載入...
3-羟基异丁酰辅酶A水解酶缺乏症一例诊治体会并文献复习
A case of 3-hydroxyisobutyryl-CoA hydrolase deficiency was reported, and its clinical features, gene mutation characteristics, and diagnosis and treatment were analyzed with reference to related literature. The patient aged 1 year and 6 months had developmental regression and paroxysmal dystonia aft...
Na minha lista:
| 發表在: | Zhongguo Dang Dai Er Ke Za Zhi |
|---|---|
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
中国当代儿科杂志编辑部
2018
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7389760/ https://ncbi.nlm.nih.gov/pubmed/30111474 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7499/j.issn.1008-8830.2018.08.009 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|