Frequency of the G6PD nt 1311 C/T polymorphism in English and Iranian populations: Relevance to studies of X chromosome inactivation

11Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

Abstract

X chromosome inactivation is widely studied using DNA sequence polymorphisms and DNA methylation as a surrogate measure of inactivation, but the correlation of methylation with inactivation is not perfect. Thus, it may be better to study sequence polymorphisms expressed in the mRNA. A recent paper reported use of a silent C/T polymorphism at nt 1311 of the G6PD cDNA, and this polymorphism was reported to have a frequency of 40% in all ethnic groups. We have screened 218 English and 50 Iranian subjects by PCR and restriction digestion; 53/218 (24%) British and 22/50 (44%) Iranian subjects were heterozygous. Thus, X inactivation studies using this polymorphism may be useful in some populations, including Iran, but much less so in the UK.

Cite

CITATION STYLE

APA

Mortazavi, Y., Chopra, R., Gordon-Smith, E. C., & Rutherford, T. R. (1997). Frequency of the G6PD nt 1311 C/T polymorphism in English and Iranian populations: Relevance to studies of X chromosome inactivation. Journal of Medical Genetics, 34(12), 1028–1029. https://doi.org/10.1136/jmg.34.12.1028

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free