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Mild thalassemia: the result of interactions of alpha and beta thalassemia genes

Homozygous thalassemia is due to inherited unbalanced synthesis of the α- or β-chains of hemoglobin. Clinical severity may be in part related to the extent of α:β imbalance. Two families are presented that illustrate this concept. Thalassemia in these individuals was evaluated by clinical and geneti...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Kan, Yuet Wai, Nathan, David G.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1970
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC322517/
https://ncbi.nlm.nih.gov/pubmed/5443168
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