Genetic links to congenital heart defects: A comprehensive meta-analysis of MTHFD1 and CBS polymorphisms
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Elsevier BV
Reference29 articles.
1. Relationship of MTHFD1 G1958A and CBS 844ins68 polymorphism with congenital heart defects in north Indian population (Jammu and Kashmir): a case-control study;Bala;Indian J. Med. Sci.,2022
2. Genetic testing in congenital heart disease: a clinical approach;Chaix;World J. Cardiol.,2016
3. Disruption of the MTHFD1 gene reveals a monofunctional 10-formyltetrahydrofolate synthetase in mammalian mitochondria;Christensen;J. Biol. Chem.,2005
4. The MTHFD1 p.Arg653Gln variant alters enzyme function and increase risk for congenital heart defects;Christensen;Hum. Mutat.,2008
5. The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects;Christensen;Hum. Mutat.,2009
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