Identification of variants in 94 Chinese patients with hereditary spherocytosis by next‐generation sequencing-Reference-Cited by-同舟云学术

Identification of variants in 94 Chinese patients with hereditary spherocytosis by next‐generation sequencing

Published:2022-10-21 Issue:1 Volume:103 Page:67-78
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Wang Wen‐Juan¹,Xie Jun‐dan¹,Yao Hong¹,Ding Zi‐xuan¹,Jiang Ai‐rui¹,Ma Liang¹,Shen Hong‐jie¹,Chen Su‐ning¹

Affiliation:

1. National Clinical Research Center for Hematologic Diseases, Key Laboratory of Thrombosis and Hemostasis of Ministry of Health, Collaborative Innovation Center of Hematology The First Affiliated Hospital of Soochow University, Jiangsu Institute of Hematology Suzhou China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14244

Reference46 articles.

1. Inherited hemolytic anemia: a possessive beginner’s guide

2. Hereditary spherocytosis—defects in proteins that connect the membrane skeleton to the lipid bilayer

3. Abnormalities of the Erythrocyte Membrane

4. A systematic review of hereditary spherocytosis reported in Chinese biomedical journals from 1978 to 2013 and estimation of the prevalence of the disease using a disease model

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