Feasibility of combining short tandem repeats (STRs) haplotyping with preimplantation genetic diagnosis (PGD) in screening for beta thalassemia

β-thalassemia is an autosomal recessive disease with the reduction or absence in the production of β-globin chain in the hemoglobin, which is caused by mutations in the Hemoglobin subunit beta (HBB) gene. In Vietnam, the number of β-thalassemia carriers range from 1.5 to 25.0%, depending on ethnic a...

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Detalles Bibliográficos
Autores principales: Vuong, Vu Viet Ha, Tran, Thinh Huy, Nguyen, Phuoc-Dung, Thi, Nha Nguyen, Le Thi, Phuong, Minh Nguyet, Dang Thi, Nguyen, Manh-Ha, Bui, The-Hung, Ta, Thanh Van, Tran, Van-Khanh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9728894/
https://www.ncbi.nlm.nih.gov/pubmed/36476827
http://dx.doi.org/10.1371/journal.pone.0278539

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9728894/
https://www.ncbi.nlm.nih.gov/pubmed/36476827
http://dx.doi.org/10.1371/journal.pone.0278539

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