Development of allelic discrimination assay to detect Mediterranean G6PD mutation and its linked inheritance with normal vision and/colorblindness loci for 4 generations among Egyptian and Emirati families

G6PD deficiency c563T is the most common inherent blood disease among the Mediterranean populations and its molecular diagnosis is critical as the enzyme assay fails for heterozygous individuals. The purpose of the study is to estimate the ubiquity of the heterozygous G6PD Med (c563T) variants among...

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Detalles Bibliográficos
Autores principales: Maloukh, Lina, Kumarappan, Alagappan, El-Din El-Wakil, Houssam, Al-Kamali, Fatima, Gomma, Fatma, Akhondi, Amin, T.V., Rajya Lakshmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381007/
https://www.ncbi.nlm.nih.gov/pubmed/34466078
http://dx.doi.org/10.1016/j.sjbs.2021.05.014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381007/
https://www.ncbi.nlm.nih.gov/pubmed/34466078
http://dx.doi.org/10.1016/j.sjbs.2021.05.014

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