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The Search for Genetic Modifiers of Disease Severity in the β-Hemoglobinopathies
Sickle cell disease (SCD) and β-thalassemia, two monogenic diseases caused by mutations in the β-globin gene, affect millions of individuals worldwide. These hemoglobin disorders are characterized by extreme clinical heterogeneity, complicating patient management and treatment. A better understandin...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2012
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3475403/ https://ncbi.nlm.nih.gov/pubmed/23028136 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/cshperspect.a015032 |
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