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Fannin-Lubbock-I [α2β2(119(GLY>ASP))], a rare mutation in the beta-globin gene, has been detected for the first time in a Hindu Brahmin family in West Bengal, India
This study aims to describe the hemoglobin Fannin-Lubbock-I, which has a rare mutation substituting the amino acid glycine with aspartic acid at codon 119 of the β-globin chain. A Bengalee Hindu Brahmin family from Kolkata in West Bengal was the focus of this study. Molecular analysis using ARMS-PCR...
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| Pubblicato in: | Cell Mol Biol Lett |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Versita
2014
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6275635/ https://ncbi.nlm.nih.gov/pubmed/24802353 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2478/s11658-014-0192-6 |
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