Identification of five rare mutations including a novel frameshift mutation causing β0-thalassemia in Thai patients with β0-thalassemia/hemoglobin E disease-Reference-Cited by-同舟云学术

Identification of five rare mutations including a novel frameshift mutation causing β0-thalassemia in Thai patients with β0-thalassemia/hemoglobin E disease

Published:1992-08 Issue:4 Volume:1139 Page:280-286
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Winichagoon Pranee,Fucharoen Suthat,Wilairat Prapon,Chihara Kazuo,Fukumaki Yasuyuki,Wasi Prawase

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference24 articles.

1. Hemoglobinopathies in Southeast Asia

2. The molecular basis of alpha-thalassaemia in Thailand.

3. Molecular basis of βo-thalassemia/HbE disease in Thailand

4. Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide Probes

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