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Article

Correlation of beta-thalassemia mutations with alpha-thalassemia: an experience of the southwestern region of Iran.

Hematology (Amsterdam, Netherlands) - 1 Dec 2010

Rahim Fakher

Abstract excerpt

BACKGROUND AND AIMS: Thalassemias are the commonest monogenic diseases worldwide. Mutations in genes coding for the globin proteins that alter protein output, produce the thalassemia syndromes. This study aimed to present the cases of alpha-thalassemia in beta-thalassemic patients from Khuzestan province in Iran. MATERIALS AND METHODS: A total of 227 subjects (10-45 years, mean age of 14·8 years) including...

Topics

Adolescent
Adult
Child
Family
Female
Genetic Counseling
Genotype
Humans
Iran
Male
Middle Aged
Mutation
Polymerase Chain Reaction

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Prenatal Diagnosis

Young Adult

alpha-Thalassemia

beta-Thalassemia

Source

Identifiers

PMID: 21114907
DOI: 10.1179/102453310X12719010991821

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