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dc.contributor.author |
Bounab, Meriem |
|
dc.contributor.author |
Lamrani, Abir |
|
dc.contributor.author |
Benseghier, Salima (Encadreur) |
|
dc.date.accessioned |
2021-04-11T09:16:52Z |
|
dc.date.available |
2021-04-11T09:16:52Z |
|
dc.date.issued |
2020 |
|
dc.identifier.uri |
http://dspace.univ-jijel.dz:8080/xmlui/handle/123456789/7658 |
|
dc.description |
Speciality: Molecular and Cellular Biology |
fr_FR |
dc.description.abstract |
Glucose-6-phosphate dehydrogenase (G6PD) is a critical enzyme for protecting red
blood cells from oxidative damage. G6PD deficiency is an X-linked recessive disorder
caused by mutations in the G6PD gene and affects nearly 400 million people worldwide.
Among G6PD deficient individuals, it is common to experience the premature breakdown of
red blood cells in the face of oxidative stress.
It has been found in the literature that the African variants of G6PD A- is more
common in the Arab countries than in the Mediterranean’s, but its percentage is low
compared to other forms of G6PD deficiency. |
fr_FR |
dc.language.iso |
en |
fr_FR |
dc.publisher |
Université de jijel |
fr_FR |
dc.subject |
G6PD deficiency |
fr_FR |
dc.subject |
G6PD A |
fr_FR |
dc.subject |
Arab and Mediterranean countries |
fr_FR |
dc.title |
Glucose-6-phosphate dehydrogenase : distribution of the African form in the Arab and Mediterranean countries |
fr_FR |
dc.type |
Thesis |
fr_FR |
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