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Hematology Volume 25, 2020 - Issue 1
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Research Article

Hereditary spherocytosis overlooked for 7 years in a pediatric patient with β-thalassemia trait and novel compound heterozygous mutations of SPTA1 gene

Min Chena Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, People’s Republic of ChinaView further author information
,
Yu-Ping Yea Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, People’s Republic of ChinaView further author information
,
Lin Liaoa Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, People’s Republic of ChinaView further author information
,
Xue-Lian Denga Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, People’s Republic of ChinaView further author information
,
Yu-Ling Qiub Department of Pediatrics, First Affiliated Hospital of Guangxi Medical University, Nanning, People’s Republic of ChinaView further author information
&
Fa-Quan Lina Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, People’s Republic of ChinaCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0002-8631-4339View further author information
ORCID Icon
Pages 438-445 | Published online: 19 Nov 2020

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