Mutation analysis of β-thalassemia in East-Western Indian population: a recent molecular approach

BACKGROUND: β-Thalassemia is the most prevalent genetic disorder in India. Its traits and coinheritance vary from mild to severe conditions, resulting in thalassemia minor, intermediate, and major, depending upon many factors. PURPOSE: The objective of this study was to identify the incidence of β-t...

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Detalhes bibliográficos
Publicado no:Appl Clin Genet
Main Authors: Shah, Parth S, Shah, Nidhi D, Ray, Hari Shankar P, Khatri, Nikunj B, Vaghasia, Ketan K, Raval, Rutvik J, Shah, Sandip C, Rao, Mandava V
Formato: Artigo
Idioma:Inglês
Publicado em: Dove Medical Press 2017
Assuntos:
Original Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5436775/
https://ncbi.nlm.nih.gov/pubmed/28546763
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S127531
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