Xmn1-158 γGVariant in B-Thalassemia Intermediate Patients in South-East of Iran

Background: Xmn-1 polymorphism of 𝜸(G)globin gene (HBG2) is a prominent quantitative trait loci (QTL) in β-thalassemia intermediate (β-TI). In current study, we evaluated the frequency of Xmn-1 polymorphism and its association with β-globin gene (HBB) alleles and Hb F level in β-TI patients in Sista...

Descripción completa

Detalles Bibliográficos
Autores principales: Miri-Moghaddam, Ebrahim, Bahrami, Sara, Naderi, Majid, Bazi, Ali, Karimipoor, Morteza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575729/
https://www.ncbi.nlm.nih.gov/pubmed/28875012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575729/
https://www.ncbi.nlm.nih.gov/pubmed/28875012

Ejemplares similares