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-Reference-Cited by-同舟云学术

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

Published:2021-09 Issue:9 Volume:28 Page:5028-5033
ISSN:1319-562X
Container-title:Saudi Journal of Biological Sciences
language:en
Short-container-title:Saudi Journal of Biological Sciences

Author:

Maloukh Lina,Kumarappan Alagappan,El-Din El-Wakil Houssam,Al-Kamali Fatima,Gomma Fatma,Akhondi Amin,T.V. Rajya Lakshmi

Publisher

Elsevier BV

Subject

General Agricultural and Biological Sciences

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3. Molecular characterization of glucose-6-phosphate dehydrogenase deficient variants in Baghdad city - Iraq;Al-Musawi;BMC Hematol.,2012

4. Arnaout, H.H., El-Gharbawy, N.M., Shaheen, I.A., Afifi, R.A., Abd EL-Dayem, O.Y., 2011. Incidence and Association of 563 C/T Mediterranean and the Silent 1311C/T G6PD Mutations in G6PD-deficient Egyptian Children. Lab. Med. 42(6), 355–360.

5. A practical guide for colour-vision examination: report of the Standardization Committee of the International Research group on colour-vision deficiencies;Birch;Ophthalmic Physiol. Opt.,1985

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