Neonatal Hyperbilirubinemia in infants with G6PD c.563C > T Variant
Background There is a strong correlation between glucose-6-phosphate dehydrogenase
(G6PD) deficiency and neonatal hyperbilirubinemia with a rare but potential threat of …
(G6PD) deficiency and neonatal hyperbilirubinemia with a rare but potential threat of …
Prevalence and molecular characterization of Glucose-6-Phosphate dehydrogenase deficient variants among the Kurdish population of Northern Iraq
Abstract Background Glucose-6-Phosphate dehydrogenase (G6PD) is a key enzyme of the
pentose monophosphate pathway, and its deficiency is the most common inherited …
pentose monophosphate pathway, and its deficiency is the most common inherited …
[HTML][HTML] G6PD enzyme deficiency in neonatal pathologic hyperbilirubinemia in Yazd
M Pahlavanzadeh, S Hekmatimoghaddam… - Iranian journal of …, 2013 - ncbi.nlm.nih.gov
Background About 7.5% of the world population carries one or two deficient copy of glucose-
6-phosphate dehydrogenase (G6PD) genes. According to WHO, its prevalence in Iran is 10 …
6-phosphate dehydrogenase (G6PD) genes. According to WHO, its prevalence in Iran is 10 …
Molecular characterization of glucose‐6‐phosphate dehydrogenase deficiency in Pakistani population
Summary Introduction: Glucose‐6‐phosphate dehydrogenase (G6PD; EC 1.1. 1.49)
deficiency is the commonest inborn error of metabolism with more than 140 genetic variants …
deficiency is the commonest inborn error of metabolism with more than 140 genetic variants …
[HTML][HTML] Next generation sequencing (NGS) in glucose-6-phosphate dehydrogenase (G6PD) deficiency studies
NM Bogari - Bioinformation, 2016 - ncbi.nlm.nih.gov
Abstract Glucose-6-phosphate dehydrogenase (G6PD) deficiency is commonly observed in
human males. It is a genetic disorder affecting the red blood cells. The diagnosis of G6PD is …
human males. It is a genetic disorder affecting the red blood cells. The diagnosis of G6PD is …
[PDF][PDF] Glucose 6-phosphate dehydrogenase deficiency in Tehran, Zanjan and Sistan-Balouchestan provinces: prevalence and frequency of Mediterranean variant of …
Y Mortazavi, MF MIRZA, AM TEREMAHI, ME MIRI… - 2010 - sid.ir
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an enzymopathy affecting about
400 million people worldwide. The distribution of G6PD deficiency and the molecular …
400 million people worldwide. The distribution of G6PD deficiency and the molecular …
Common mutations in G6PD of Vietnamese-Kinh deficient patients
This study was conducted to identify the common mutations occurring within the G6PD gene
in the G6PD-Vietnamese deficient patients, which may be the main causative mutations of …
in the G6PD-Vietnamese deficient patients, which may be the main causative mutations of …
[HTML][HTML] Identification of mutation of Glucose-6-Phosphate Dehy–drogenase (G6PD) in Iran: Meta-analysis study
M Moosazadeh, M Nekoei-Moghadam… - Iranian Journal of …, 2013 - ncbi.nlm.nih.gov
Background Glucose-6-phosphate dehydrogenase is one of the most common genetic
deficiencies, which approximately 400 million people in the world suffer from. According to …
deficiencies, which approximately 400 million people in the world suffer from. According to …
Molecular basis of G6PD deficiency: current status and its perspective
DMR NOURI, PM DANESH - 2008 - sid.ir
Abstract GLUCOSE-6-PHOSPHATE DEHYDROGENASE is an essential enzyme to cell
growth. Its deficiency of enzyme plays an important role in SENESCENCE and death …
growth. Its deficiency of enzyme plays an important role in SENESCENCE and death …
The prevalence of mediterranean mutation of glucose-6-phosphate dehydrogenase (G6PD) in Zahedan
: Background: glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common
genetic defects in the world, so that more than 400 million people in worldwide are affected …
genetic defects in the world, so that more than 400 million people in worldwide are affected …