Thalassemia Major and Intermedia Patients in East Java do not Show Fetal Hemoglobin Level Difference in Relation to XMNI Polymorphism

INTRODUCTION: Thalassemia is a genetic disorder, which shows, varies phenotype due to genetic modifier. XmnI is one of the genetic modifiers which affect clinical severity in thalassemia. XmnI polymorphism may increase HbF production beyond fetal life, thus ameliorating the clinical phenotype. AIM:...

Descripción completa

Detalles Bibliográficos
Autores principales: Wulandari, Retno Dwi, Lyrawati, Diana, Fatchiyah, Fatchiyah, Fitri, Loeki Enggar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences of Bosnia and Herzegovina 2020
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296421/
https://www.ncbi.nlm.nih.gov/pubmed/32577047
http://dx.doi.org/10.5455/medarh.2020.74.90-94

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7296421/
https://www.ncbi.nlm.nih.gov/pubmed/32577047
http://dx.doi.org/10.5455/medarh.2020.74.90-94

Ejemplares similares