Evaluation of High Resolution Melting for MTHFR C677T Genotyping in Congenital Heart Disease-Reference-Cited by-同舟云学术

Evaluation of High Resolution Melting for MTHFR C677T Genotyping in Congenital Heart Disease

Published:2016-03-18 Issue:3 Volume:11 Page:e0151140
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Wang Ying,Zhang Haiyan,Yue Shuying,Zhang Kun,Wang Hui,Dong Rui,Yang Xiaomeng,Liu Yi,Ma Yanhui

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference23 articles.

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4. Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease;R Junker;Cardiovasc Res,2001

5. MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases;HE Zidan;Gene,2013

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1. Congenital septal defects in Karachi, Pakistan: an update of mutational screening by high-resolution melting (HRM) analysis of MTHFR C677T;Human Genomics;2024-01-29

2. “Association of MTHFR and MS/MTR gene polymorphisms with congenital heart defects in North Indian population (Jammu and Kashmir): a case–control study encompassing meta-analysis and trial sequential analysis”;BMC Pediatrics;2022-04-25

3. Association Between MTHFR C677T Polymorphism and Susceptibility to Autism Spectrum Disorders: A Meta-Analysis in Chinese Han Population;Frontiers in Pediatrics;2021-03-10

4. Association Between MTHFR C677T Polymorphism and Congenital Heart Disease;International Heart Journal;2020-05-30

5. Two Common MTHFR Gene Polymorphisms (C677T and A1298C) and Fetal Congenital Heart Disease Risk: An Updated Meta-Analysis with Trial Sequential Analysis;Cellular Physiology and Biochemistry;2018