Identification of a novel ANK1 mutation in a Chinese family with hereditary spherocytosis: A case report-Reference-Cited by-同舟云学术

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Identification of a novel ANK1 mutation in a Chinese family with hereditary spherocytosis: A case report

Published:2022-11-16 Issue:1 Volume:25 Page:
ISSN:1792-0981
Container-title:Experimental and Therapeutic Medicine
language:
Short-container-title:Exp Ther Med

Author:

Zhu Xiaoning¹,Peng Mengyun¹,Yin Yue¹,Zhang Yurong¹,Zheng Ding¹,Peng Zhaoxuan¹,Cheng Jun²,Yang Song²,Wang Jing¹

Affiliation:

1. Department of Hepatobiliary Disease, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, Sichuan 646000, P.R. China

2. Center of Liver Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing 100020, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Immunology and Microbiology (miscellaneous),General Medicine

Cited by 1 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 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

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