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Variable Clinical Phenotypes of α-Thalassemia Syndromes
Genetic mutations of the α genes are common worldwide. In Asia and particularly Southeast Asia, they can result in clinically significant types of α-thalassemia, namely hemoglobin (Hb) H disease and Hb Bart's hydrops fetalis. The latter is generally a fatal intrauterine condition, while Hb H di...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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TheScientificWorldJOURNAL
2009
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5823233/ https://www.ncbi.nlm.nih.gov/pubmed/19618088 http://dx.doi.org/10.1100/tsw.2009.69 |