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Co-inheritance of HbD (Iran)/Beta Thalassemia IVS1–5 (G > C) Trait in a Punjabi Lady with Diabetes
The present report describes the molecular study of HbD (Iran) (beta) 22 Glu → Gln associated with β-Thalassemia IVS1–5 (G > C) found in India, and the first case in which mutation has been identified using mass spectrometry. Given the apparent ethnic origin and the mobility of the variant hemogl...
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| Glavni autori: | , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Springer-Verlag
2012
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3358370/ https://ncbi.nlm.nih.gov/pubmed/23543793 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12291-012-0201-3 |
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