Targeted next-generation sequencing identifies a novel nonsense mutation in ANK1 for hereditary spherocytosis: A case report
Author:
Publisher
Baishideng Publishing Group Inc.
Subject
General Medicine
Reference19 articles.
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Cited by 3 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. Clinical and genetic diagnosis of two Turkish patients with hereditary spherocytosis;The European Research Journal;2024-08-20
2. Clinical manifestations of 17 Chinese children with hereditary spherocytosis caused by novel mutations of the ANK1 gene and phenotypic analysis;Frontiers in Genetics;2023-02-01
3. A novel splicing mutation of ANK1 is associated with phenotypic heterogeneity of hereditary spherocytosis in a Chinese family;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2023-01
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