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...

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Detalles Bibliográficos
Autores principales: Chen, Meihuan, Zhang, Min, Chen, Lingji, Lin, Na, Wang, Yan, Xu, Liangpu, Huang, Hailong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Research Articles
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

Internet

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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