Molecular Basis of β-Thalassemia in Karnataka, India-Reference-Cited by-同舟云学术

Molecular Basis of β-Thalassemia in Karnataka, India

Published:2012-02 Issue:2 Volume:16 Page:138-141
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Kulkarni Gururaj D.¹,Kulkarni Suyamindra S.¹,Kadakol Gurushantappa S.¹,Kulkarni Bhushan B.²,Kyamangoudar Prakashgouda H.¹,Lakkakula Bhaskar V.K.S.³,Thangaraj Kumarasamy⁴,Shepur Tipperudra A.⁵,Kulkarni Muralidhar L.⁶,Gai Pramod B.¹

Affiliation:

1. Research Center for DNA Diagnostics, Department of Applied Genetics, Karnatak University, Dharwad, Karnataka, India.

2. Department of Biotechnology, P.C. Jabin Science College, Hubli, Karnataka, India.

3. Department of Biomedical Sciences, Sri Ramachandra University, Porur, Chennai, Tamil Nadu, India.

4. Center for Cellular and Molecular Biology, Hyderabad, Andhra Pradesh, India.

5. Department of Pediatrics, Karnataka Institute of Medical Sciences, Hubli, Karnataka, India.

6. Department of Pediatrics, J.J.M. Medical College, Davanagere, Karnataka, India.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2011.0035

Reference35 articles.

1. Geographic and Ethnic Distribution of β-Thalassemia Mutations in Uttar Pradesh, India

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

3. Molecular genetic analyses of β-thalassemia in South India reveals rare mutations in the β-globin gene

4. Bhasin MK, Walter H, Danker-Hopfe H (1994) People of India: An investigation of biological variability in ecological, ethno-economic and linguistic group. Kamala Raj Enterprises, Delhi.

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