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Genetic research and clinical analysis of β‐globin gene cluster deletions in the Chinese population of Fujian province: A 14‐year single‐center experience
BACKGROUND: Heterozygotes of HPFH and δβ thalassemia are clinically asymptomatic or have mild hemoglobin (Hb) values. However, when both HPFH and δβ‐thalassemia are coinherited with heterozygous β‐thalassemia, patients may progress to a clinical phenotype of thalassemia intermedia or thalassemia maj...
Autores principales: | Chen, Meihuan, Zhang, Min, Chen, Lingji, Lin, Na, Wang, Yan, Xu, Liangpu, Huang, Hailong |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8842190/ https://www.ncbi.nlm.nih.gov/pubmed/34951062 http://dx.doi.org/10.1002/jcla.24181 |
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