載入...
Point-of-Care Testing for G6PD Deficiency: Opportunities for Screening
Glucose-6-phosphate dehydrogenase (G6PD) deficiency, an X-linked genetic disorder, is associated with increased risk of jaundice and kernicterus at birth. G6PD deficiency can manifest later in life as severe hemolysis, when the individual is exposed to oxidative agents that range from foods such as...
Na minha lista:
| 發表在: | Int J Neonatal Screen |
|---|---|
| Main Authors: | , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
MDPI
2018
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6832607/ https://ncbi.nlm.nih.gov/pubmed/31709308 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijns4040034 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|