“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”

BACKGROUND: The risk of Congenital Heart Defects (CHD) is greatly influenced by variants within the genes involved in folate-homocysteine metabolism. Polymorphism in MTHFR (C677T and G1793A) and MS/MTR (A2756G) genes increases the risk of developing CHD risk, but results are controversial. Therefore...

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Detalles Bibliográficos
Autores principales: Raina, Jyotdeep Kour, Panjaliya, Rakesh Kumar, Dogra, Vikas, Sharma, Sushil, Anupriya, Kumar, Parvinder
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036697/
https://www.ncbi.nlm.nih.gov/pubmed/35468734
http://dx.doi.org/10.1186/s12887-022-03227-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036697/
https://www.ncbi.nlm.nih.gov/pubmed/35468734
http://dx.doi.org/10.1186/s12887-022-03227-z

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