Ameliorating β-thalassaemia by manipulating expression of the α-globin gene

<p>β-Thalassaemia is a disorder of haemoglobin production characterised by severe anaemia requiring life-long blood transfusions. The common genetic defects are predominantly based in and around the β-globin gene resulting in reduced or absent β-globin chain synthesis. The resultant excess of...

Бүрэн тодорхойлолт

Номзүйн дэлгэрэнгүй
Үндсэн зохиолч: Mettananda, S
Бусад зохиолчид: Higgs, D
Формат: Дипломын ажил
Хэл сонгох:English
Хэвлэсэн: 2015
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