載入...
Molecular Characterization of G6PD Deficiency: Report of Three Novel G6PD Variants
G6PD deficiency is a monogenic, X-linked genetic defect with a worldwide prevalence of around 400 million people and an overall prevalence of 8.5% in India. Hemolytic anemia is encountered in only a small proportion of patients with G6PD variants and is usually triggered by some exogenous agent. Alt...
Na minha lista:
| 發表在: | Indian J Hematol Blood Transfus |
|---|---|
| Main Authors: | , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Springer India
2019
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7229042/ https://ncbi.nlm.nih.gov/pubmed/32425388 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-019-01205-7 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|