Identification of a novel pre-terminating mutation in human HBB gene as a cause of β0-thalassemia phenotype.
Year: 2019
Type: article
Abstract: -thal and is useful for genetic counseling and prenatal screening.
Source: Europe PMC (PubMed Central)
Authors: Liangpu Xu, Meihuan Chen, Hailong Huang, Na Lin, Lingji Chen, Yan Wang, Min Zhang, Deqin He, Yuan Lin
Institution: Fujian Medical University
Language: English
Subfield: Genetics (clinical)
Field: Medicine
Domain: Health Sciences
Open Access status: green
OpenAlex ID: W3014600682