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
Differences in the frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene among the Lebanese population
β Scribed by Wassim Y. Almawi; Ramzi R. Finan; Hala Tamim; Jocelyn L. Daccache; Noha Irani-Hakime
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 59 KB
- Volume
- 76
- Category
- Article
- ISSN
- 0361-8609
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