Compound Heterozygosity of β-Thalassemia Traits of HBB Gene in a Family: A Case Report-Reference-Cited by-同舟云学术

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Compound Heterozygosity of β-Thalassemia Traits of HBB Gene in a Family: A Case Report

Published:2017-04-03 Issue:2 Volume:17 Page:72-75
ISSN:0972-3757
Container-title:International Journal of Human Genetics
language:en
Short-container-title:International Journal of Human Genetics

Author:

Shah Parth S.¹,Shah Nidhi D.¹,Ray Hari Shankar P.¹,Khatri Nikunj B.¹,Vaghasia Ketan K.¹,Shah Sandip C.¹,Rao Mandava V.¹²

Affiliation:

1. Supratech Genopath Laboratory and Research Institute, Ahmedabad, Gujarat, India

2. School of Sciences, Gujarat University, Ahmedabad, Gujarat, India

Publisher

Kamla Raj Enterprises

Subject

Genetics(clinical),Genetics

Link

https://www.tandfonline.com/doi/pdf/10.1080/09723757.2017.1347164

Reference11 articles.

1. Clinical and haematological features in a compound heterozygote (HBB:c.92 + 5G > C/HBB:c.93-2A > C) case of thalassaemia major

2. Compound heterozygous β+ β0 mutation of HBB gene leading to β-thalassemia major in a Gujarati family — A case study

3. Thalassaemia

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