2020
DOI: 10.1007/s12291-020-00890-w
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C677T MTHFR Gene Polymorphism is Contributing Factor in Development of Renal Impairment in Young Hypertensive Patients

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Cited by 4 publications
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“…The C677T mutation is the most common missense mutation in MTHFR ; it can occur stably in populations around the globe and has a worldwide distribution of high frequency. In normal populations, the frequency of TT homozygotes is approximately 4% in Egyptian ( 10 ) and approximately 23% in Italians in Europe ( 11 ), while the T allele frequency is at a higher level of 41% in the Chinese population ( 8 ). According to Hou ( 12 ), the T allele frequency of healthy pregnant women is 27%.…”
Section: Discussionmentioning
confidence: 99%
“…The C677T mutation is the most common missense mutation in MTHFR ; it can occur stably in populations around the globe and has a worldwide distribution of high frequency. In normal populations, the frequency of TT homozygotes is approximately 4% in Egyptian ( 10 ) and approximately 23% in Italians in Europe ( 11 ), while the T allele frequency is at a higher level of 41% in the Chinese population ( 8 ). According to Hou ( 12 ), the T allele frequency of healthy pregnant women is 27%.…”
Section: Discussionmentioning
confidence: 99%