Amelioration of Sardinian β(0) thalassemia by genetic modifiers

Sardinian β-thalassemia patients all are homozygotes for the same null allele in the β-globin gene, but the clinical manifestations are extremely variable in severity. Previous studies have shown that the coinheritance of α-thalassemia or the presence of genetic variants that sustain fetal hemoglobi...

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Hlavní autoři: Galanello, Renzo, Sanna, Serena, Perseu, Lucia, Sollaino, Maria Carla, Satta, Stefania, Lai, Maria Eliana, Barella, Susanna, Uda, Manuela, Usala, Gianluca, Abecasis, Goncalo R., Cao, Antonio
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society of Hematology 2009
Témata:
Red Cells, Iron, and Erythropoiesis
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2925722/
https://ncbi.nlm.nih.gov/pubmed/19696200
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2009-04-217901
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