Literature DB >> 30988594

A Novel G6PD p. Gly 321 Val Mutation Causing Severe Hemolysis in an Indian Infant.

R Devendra1, P Warang1, V Gupta1, A Chiddarwar1, P Kedar1, M B Agarwal2, M B Mukherjee1.   

Abstract

Entities:  

Year:  2018        PMID： 30988594      PMCID： PMC6439128          DOI： 10.1007/s12288-018-1049-3

Source DB:  PubMed          Journal:  Indian J Hematol Blood Transfus        ISSN： 0971-4502            Impact factor:   0.900


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  4 in total

Review 1.  The genetics of glucose-6-phosphate dehydrogenase deficiency.

Authors:  E Beutler
Journal:  Semin Hematol       Date:  1990-04       Impact factor: 3.851

2.  Human glucose-6-phosphate dehydrogenase: the crystal structure reveals a structural NADP(+) molecule and provides insights into enzyme deficiency.

Authors:  S W Au; S Gover; V M Lam; M J Adams
Journal:  Structure       Date:  2000-03-15       Impact factor: 5.006

Review 3.  G6PD deficiency.

Authors:  E Beutler
Journal:  Blood       Date:  1994-12-01       Impact factor: 22.113

4.  Glucose-6-phosphate dehydrogenase (G6PD) mutations database: review of the "old" and update of the new mutations.

Authors:  Angelo Minucci; Kamran Moradkhani; Ming Jing Hwang; Cecilia Zuppi; Bruno Giardina; Ettore Capoluongo
Journal:  Blood Cells Mol Dis       Date:  2012-01-30       Impact factor: 3.039
  4 in total

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