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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
Autori principali: Basak, Jayasri, Bhattacharyya, Deboshree M., Mukhopadhyay, Ashis
Natura: Artigo
Lingua:Inglês
Pubblicazione: Versita 2014
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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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