The Correlation Between Clinical Phenotype and Genotype of Hereditary Spherocytosis-Reference-Cited by-同舟云学术

The Correlation Between Clinical Phenotype and Genotype of Hereditary Spherocytosis

Published:2024-01-01 Issue:1 Volume:28 Page:33-38
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Shen Hao¹^ORCID,Gao Zhigang²,Ye Qing¹

Affiliation:

1. Department of Clinical Laboratory, The Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Hangzhou, China.

2. Department of Pediatric General Surgery, The Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Hangzhou, China.

Publisher

Mary Ann Liebert Inc

Link

https://www.liebertpub.com/doi/pdf/10.1089/gtmb.2023.0307

Reference32 articles.

1. Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next‐generation sequencing: First South Asian study

2. A novel L1340P mutation in theANK1gene is associated with hereditary spherocytosis?

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

4. Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte

5. Whole exome sequencing identified a novel mutation (p.Ala1884Pro) of β-spectrin in a Chinese family with hereditary spherocytosis

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1. Correction to: The Correlation Between Clinical Phenotype and Genotype of Hereditary Spherocytosis, by Hao Shen, et al. Genet Test Mol Biomarkers 2024; (vol. 28, no. 1; 33–38); doi: 10.1089/gtmb.2023.0307;Genetic Testing and Molecular Biomarkers;2024-03-01