Frequencies and hematological manifestations of the HKαα allele in southern Chinese population.
Year: 2019
Type: article
Study design: Observational Study
Abstract: INTRODUCTION: /αα. METHODS: and α2 bands by gap-PCR, and reverse dot-blot assays were performed to detect the non-deletional α thalassemia point mutations and β thalassemia point mutations. RESULTS: genotype chose to retain the fetuses in our study. CONCLUSIONS: /αα can provide more accurate genetic diagnosis and clinical thalassemia genetic counseling.
Source: Europe PMC (PubMed Central)
Authors: Min Zhang, Hailong Huang, Meihuan Chen, Lingji Chen, Yan Wang, Na Lin, Yuan Lin, Liangpu Xu
Institution: Fujian Medical University
Language: English
Subfield: Genetics (clinical)
Field: Medicine
Domain: Health Sciences
Open Access status: green
OpenAlex ID: W3027380567