Five novel glucose-6-phosphate dehydrogenase deficiency haplotypes correlating with disease severity

Five novel glucose-6-phosphate dehydrogenase deficiency haplotypes correlating with disease severity

<p>Abstract</p> <p>Background</p> <p>Glucose-6-phosphate dehydrogenase (G6PD, EC 1.1.1.49) deficiency is caused by one or more mutations in the <it>G6PD</it> gene on chromosome X. An association between enzyme levels and gene haplotypes remains to be establi...

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Bibliographic Details
Main Authors: Dallol Ashraf, Banni Huda, Gari Mamdooh A, Al-Qahtani Mohammed H, Abuzenadeh Adel M, Al-Sayes Fatin, Chaudhary Adeel G, Bidwell Jeffrey, Kafienah Wael
Format: Article
Language:English
Published: BMC 2012-09-01
Series:Journal of Translational Medicine
Subjects:
Glucose-6-phosphate dehydrogenase
Haemolytic anaemia
DNA sequencing
Haplotype
PHASE reconstruction
Linkage analysis
Gene mutation
Online Access:http://www.translational-medicine.com/content/10/1/199

Internet

http://www.translational-medicine.com/content/10/1/199

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