Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis-Reference-Cited by-同舟云学术

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Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis

Published:2019-10-18 Issue: Volume:10 Page:
ISSN:1664-042X
Container-title:Frontiers in Physiology
language:
Short-container-title:Front. Physiol.

Author:

Chonat Satheesh,Risinger Mary,Sakthivel Haripriya,Niss Omar,Rothman Jennifer A.,Hsieh Loan,Chou Stella T.,Kwiatkowski Janet L.,Khandros Eugene,Gorman Matthew F.,Wells Donald T.,Maghathe Tamara,Dagaonkar Neha,Seu Katie G.,Zhang Kejian,Zhang Wenying,Kalfa Theodosia A.

Publisher

Frontiers Media SA

Subject

Physiology (medical),Physiology

Reference1 articles.

1. Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus;Bogardus;Haematologica,2014

Cited by 7 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. Novel mutation in alpha-spectrin gene in Saudi patients with hereditary spherocytosis;Nucleosides, Nucleotides & Nucleic Acids;2024-02-06

2. Gene expression analysis revealed downregulation of complement receptor 1 in clonal B cells in cold agglutinin disease;Clinical and Experimental Immunology;2023-12-22

3. Changes in expression levels of erythrocyte and immune-related genes are associated with high altitude polycythemia;BMC Medical Genomics;2023-07-28

4. A Novel <i>SPTA1</i> Mutation in a Patient with Hereditary Spherocytosis without a Family History and Coexisting Gilbert's Syndrome;Internal Medicine;2023-01-01

5. Diagnosis and clinical management of red cell membrane disorders;Hematology;2021-12-10

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