Genetic and phenotypic analysis of a rare asymptomatic case of a homozygous Chinese Gγ+(Aγδβ)0-thalassemia deletion in a Chinese family-Reference-Cited by-同舟云学术

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Genetic and phenotypic analysis of a rare asymptomatic case of a homozygous Chinese Gγ+(Aγδβ)0-thalassemia deletion in a Chinese family

Published:2020-02 Issue: Volume:76 Page:11-16
ISSN:0009-9120
Container-title:Clinical Biochemistry
language:en
Short-container-title:Clinical Biochemistry

Author:

Du Li,Qin Danqing,Wang Jicheng,Yu Lihua,Yao Cuize,Liu Ling,Zhang Yanxia,Hu Tingting,Yuan Tenglong,Liang Jie,Yin Aihua

Funder

National Key Research and Development Program of China

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference24 articles.

1. Thalassemia: an overview of 50 years of clinical research;Sankaran;Hematol. Oncol. Clin. North Am.,2010

2. Delta beta-thalassemia in a Mexican family: clinical differences among homozygotes;Reyes;Hemoglobin,1978

3. Gap-PCR screening for common large deletional mutations of β-globin gene cluster revealed a higher prevalence of the Turkish Inversion/Deletion (δβ)0 Mutation in Antalya;Bilgen;Turk. J. Haematol.,2016

4. Molecular analysis of the Turkish form of deletion-inversion (delta beta)(0) thalassaemia;Oner;Br. J. Haematol.,1997

5. J.M. Khunger, M. Gupta, R. Singh, et al. Haematological characterisation and molecular basis of Asian Indian inversion deletions delta Beta thalassemia: a case report. J. Clin. Diagn. Res. 2014; 8 (9): FD01-2.

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