Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis.
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Cited by 48 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
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3. Newborn hereditary elliptocytosis confirmed by familial genetic testing;International Journal of Laboratory Hematology;2019-07-09
4. Whole-exome sequencing for the genetic diagnosis of congenital red blood cell membrane disorders in Taiwan;Clinica Chimica Acta;2018-12
5. Hereditary elliptocytosis: Variable clinical severity caused by 3 variants in the α-spectrin gene;International Journal of Laboratory Hematology;2018-05-05
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