| Autor: |
Azma Raja Sabudin, Raja Zahratul, Fauzi, Alina Md, Abdul Jalil, Darnina, Ithnin, Azlin, Alauddin, Hafiza, Fook-Choe, Cheah, Ayub, Najiah-Ajlaa, Malisa, Moh Yusuf, Norunaluwar, Jalil, Ainoon, Othman |
| Předmět: |
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| Zdroj: |
Hemoglobin; Nov2019, Vol. 43 Issue 6, p312-312, 1p |
| Abstrakt: |
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme deficiency found in humans with an estimated global prevalence of 7.1%. Recently, a polymerase chain reaction (PCR)-based reverse dot-blot flow-through hybridization method, Hybribio G6PD deficiency Gene Diagnostic Kit (Chaozhou Hybribio Biochemistry Ltd., Chaozhou, Guangdong Province, China) that simultaneously screened for multiple G6PD mutations was employed at the UKM Medical Center. B KEYWORDS: b Glucose-6-phosphate dehydrogenase (G6PD) deficiency; G6PD assay kit; CareStart™ S1; flow-through hybridization; DNA sequencing. [Extracted from the article] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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