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Examinations of Methylenetetrahydrofolate Reductase C677T and A1298C Mutations—and In Utero Viability

✍ Scribed by K.A. Volcik; S.H. Blanton; H. Northrup

Book ID
117853730
Publisher
American Society of Human Genetics
Year
2001
Tongue
English
Weight
53 KB
Volume
69
Category
Article
ISSN
0002-9297

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Methylenetetrahydrofolate reductase (MTHFR): The incidence of mutations C677T and A1298C in the Ashkenazi Jewish population
✍ Rady, Peter L.; Tyring, Stephen K.; Hudnall, S. David; Vargas, Trini; Kellner, L 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 36 KB 👁 2 views

The polymorphic mutation C677T in the gene of MTHFR is considered a risk mutation for spina bifida and vascular disease. Another common mutation on the MTHFR gene, A1298C, has also been described as another risk mutation. We studied the frequencies of these two mutations on DNA samples from healthy