Prevalence and spectrum of mutations causing G6PD deficiency in Indian populations-Reference-Cited by-同舟云学术

Prevalence and spectrum of mutations causing G6PD deficiency in Indian populations

Published:2020-12 Issue: Volume:86 Page:104597
ISSN:1567-1348
Container-title:Infection, Genetics and Evolution
language:en
Short-container-title:Infection, Genetics and Evolution

Author:

Devendra Rati,Gupta Vinodkumar,Shanmugam Rajasubramaniam,Singh M.P.S.S.,Patel Purushottam,Valecha Neena,Mishra Neelima^ORCID,Ahmed Naseem,Hoti S.L.,Hegde Harsha V.,Warang Prashant,Chiddarwar Ashish,Kedar Prabhakar,Mayekar Pramod,Mukherjee Malay B.

Funder

Indian Council of Medical Research

Publisher

Elsevier BV

Subject

Infectious Diseases,Microbiology (medical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics,Microbiology

Reference56 articles.

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3. Molecular characterization of G6PD deficiency: report of three novel G6PD variants;Arunachalam;Ind. J. of Hemat. Blood Transf.,2019

4. Human glucose-6-phosphate dehydrogenase: the crystal structure reveals a structural NADP+ molecule and provides insights into enzyme deficiency;Au;Structure.,2000

5. Deficiency of G6PD observations on a sample from Bombay;Baxi;Cur. Sci.,1961

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