Cargando…
Tetra-Primer ARMS PCR Optimization for Detection of IVS-II-I (G-A) and FSC 8/9 InsG Mutations in β-Thalassemia Major Patients in Isfahan Population
BACKGROUND: β-thalassemia, a monogenic autosomal recessive disorder, is prevalent in Middle East, particularly in Iran. In Iran, near to 20 mutations in the β-globin gene are introduced as common mutations with varying incidence frequencies in each city. Therefore, detection and screening for couple...
Autores principales: | HAJIHOSEINI, Samaneh, MOTOVALI-BASHI, Majid, HONARDOOST, Mohammad Amin, ALERASOOL, Nader |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402417/ https://www.ncbi.nlm.nih.gov/pubmed/25905082 |
Ejemplares similares
-
An arylsulphatase A (ARSA) frameshift mutation (289insG) in metachromatic leukodystrophy (MLD)
por: Perkins, Kelly J, et al.
Publicado: (2005) -
The Shank3-InsG3680(+/+) mouse model of autism spectrum disorder displays auditory avoidance in a novel behavioral test
por: Gonçalves, Ana Margarida, et al.
Publicado: (2023) -
Role of XmnI(G) Polymorphism in Hydroxyurea Treatment and Fetal Hemoglobin Level at Isfahanian Intermediate β-Thalassemia Patients
por: Motovali-Bashi, Majid, et al.
Publicado: (2015) -
Genetic association of rs1520333 G/A polymorphism in the IL7 gene with multiple sclerosis susceptibility in Isfahan population
por: Ghavimi, Reza, et al.
Publicado: (2014) -
Investigation of RFLP Haplotypes β-Globin Gene Cluster in Beta-Thalassemia Patients in Central Iran
por: Sajadpour, Zahra, et al.
Publicado: (2019)