Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus-Reference-Cited by-同舟云学术

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Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus

Published:2014-06-03 Issue:9 Volume:99 Page:e168-e170
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Bogardus H.,Schulz V. P.,Maksimova Y.,Miller B. A.,Li P.,Forget B. G.,Gallagher P. G.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 10 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. Neonatal Anemia;Principles of Neonatology;2024

2. 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

3. Allogenic haematopoeitic stem cell transplant as cure for severe transfusion‐dependent non‐dominant hereditary spherocytosis due to homozygous SPTA1 mutation;Pediatric Blood & Cancer;2022-08-11

4. Exome-Based Trio Analysis for Diagnosis of the Cause of Congenital Severe Hemolytic Anemia in a Child;Transfusion Medicine and Hemotherapy;2022

5. Genetics and Genomics Approaches for Diagnosis and Research Into Hereditary Anemias;Frontiers in Physiology;2020-12-22

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