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Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects

✍ Scribed by E. Mornet; Françoise Muller; Annie Lenvoisé-Furet; Anne-Lise Delezoide; Jean-Yves Col; Brigitte Simon-Bouy; Jean-Louis Serre


Book ID
106136758
Publisher
Springer
Year
1997
Tongue
English
Weight
20 KB
Volume
100
Category
Article
ISSN
0340-6717

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Association of the C677T polymorphism in
✍ Yasue Uchida; Saiko Sugiura; Fujiko Ando; Hiroshi Shimokata; Tsutomu Nakashima 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 88 KB

## Abstract ## Objectives/Hypothesis: To investigate the recently reported association of the C677T polymorphism in the methylenetetrahydrofolate reductase (MTHFR) gene with sudden sensorineural hearing loss (SSNHL), we analyzed data from a community‐based Japanese population. ## Study Design: N