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Combined α-thalassemia and Hemoglobin J-Iran (β77 His → Asp). A Family Study in southern Iran
We report a 23-year-old man and three members of his family with Hb J-Iran confirmed by electrophoresis, chain separation by high performance liquid chromatography and sequencing. Alpha thalassemia was also confirmed in two family members. The substitution at β77 led to a higher negative charge of t...
Autores principales: | Dehghani, S J, Amiri Dashtarzhen, A, Nasirabadi, Sh, Dehbozorgian, J, Afrasiabi, A R, Morshedi, N, Imanifard, J, Mehrpoor, Sh, Gerdabi, J, Karimi, M |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kowsar
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371998/ https://www.ncbi.nlm.nih.gov/pubmed/22737531 |
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