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Methylenetetrahydrofolate reductase mutations, a genetic cause for familial recurrent neural tube defects
Methylenetetrahydrofolate reductase (MTHFR) gene mutations have been implicated as risk factors for neural tube defects (NTDs). The best-characterized MTHFR genetic mutation 677C→T is associated with a 2–4 fold increased risk of NTD if patient is homozygous for this mutation. This risk factor is mod...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3385168/ https://ncbi.nlm.nih.gov/pubmed/22754237 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.96680 |
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