A Large Cohort Study of Genotype and Phenotype Correlations of Beta- Thalassemia in Iranian Population

Background: Thalassemia syndromes are the most prevalent single gene disorders in Iran. This study aimed to evaluate the effect of different types of beta-globin gene mutations, co-inheritance of alpha-globin gene mutations and/or Xmn1 SNP on disease phenotype in a large cohort of Iranian patients....

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Detalles Bibliográficos
Autores principales: Maryami, Fereshteh, Azarkeivan, Azita, Fallah, Mohammad Sadegh, Zeinali, Sirous
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2015
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Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748687/
https://www.ncbi.nlm.nih.gov/pubmed/26865931

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