S902 THE COMPLEXITY OF GENOTYPE-PHENOTYPE CORRELATIONS IN HEREDITARY SPHEROCYTOSIS: A COHORT OF 95 PATIENTS
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Hematology
Cited by 6 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 spherocytosis due to a novel variant, p.Q1034X, in the beta subunit of the spectrin gene: A case report;Pediatric Hematology Oncology Journal;2024-09
2. 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
3. Targeted Next Generation Sequencing and Diagnosis of Congenital Hemolytic Anemias: A Three Years Experience Monocentric Study;Frontiers in Physiology;2021-05-21
4. The Interplay between Drivers of Erythropoiesis and Iron Homeostasis in Rare Hereditary Anemias: Tipping the Balance;International Journal of Molecular Sciences;2021-02-23
5. Atypical hereditary spherocytosis phenotype associated with pseudohypokalaemia and a new variant in the band 3 protein;BMJ Case Reports;2020-12
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