THE RELATION OF DIAPHORASE OF HUMAN ERYTHROCYTES TO INHERITANCE OF METHEMOGLOBINEMIA
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Cited by 174 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Hereditary Congenital Methemoglobinemia Diagnosed at the Age of 79 Years: A Case Report;Medicina;2023-03-20
2. A RARE CAUSE OF NEONATAL CYANOSIS - CONGENITAL METHEMOGLOBINEMIA — A CASE REPORT;INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH;2021-01-01
3. In silico Analysis and Molecular Modelling of NADH-cytochrome b5 Reductase 3 involved in Methemoglobinemia;International Journal of Scientific Research in Science and Technology;2020-02-15
4. Enzymopenic Congenital Methemoglobinemia in Children of the Republic of Sakha (Yakutia);Journal of Pediatric Hematology/Oncology;2017-01
5. Molecular Disorders of Red Blood Cells, Platelets, and Coagulation System;2017
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