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Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh

CONTEXT: β-thalassemia is one of the most common heterogeneous inherited single gene disorders. The disease results from one or more of 380 different mutations in the β-globin gene. Uttar Pradesh (U.P.) is the most populous state of India, comprising various ethnic groups and Bareilly is one of the...

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Detalhes bibliográficos
Main Authors: Christopher, Ajay F., Kumari, Anita, Chaudhary, Sunali, Hora, Sandhya, Ali, Ziledar, Agrawal, Satish C.
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2013
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3758729/
https://ncbi.nlm.nih.gov/pubmed/24019624
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.116119
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