Characterization of β-Thalassemia Mutations Among the Japanese-Reference-Cited by-同舟云学术

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Characterization of β-Thalassemia Mutations Among the Japanese

Published:1989-01 Issue:7-8 Volume:13 Page:657-670
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Hattori Y.,Yamane A.,Yamashiro Y.,Matsuno Y.,Yammoto Ki.,Yamamoto Ku.,Ohba Y.,Miyaji T.

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630268908998843

Reference24 articles.

1. A novel mutation in the TATA box in a Japanese patient with beta +- thalassemia

2. A β+-Thalassemia (Codon 24, GGT → GGA) Found in a Japanese

3. A novel globin structural mutant, Showa-Yakushiji (beta 110 Leu-Pro) causing a beta-thalassemia phenotype

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1. Global distribution of β-thalassemia mutations: An update;Gene;2024-02

2. Spectrum of HBB gene mutations among 696 β–thalassemia patients and carriers in Southern Vietnam;Molecular Biology Reports;2022-01-13

3. Occurrence of the Codon 24 (A > T) Mutation in the Mauritanian Population;Hemoglobin;2015-06-05

4. Is the Poly A (T>C) Mutation a Causative Factor For Misdiagnosis in Second Trimester Prenatal Diagnosis of β-Thalassemia by Fetal Blood Analysis on High Performance Liquid Chromatography?;Hemoglobin;2012-02

5. Human Hemoglobin;Vogel and Motulsky's Human Genetics;2010

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