Methylenetetrahydrofolate reductase C677T gene polymorphism in turkish patients with polycystic ovary syndrome
β Scribed by Muammer Karadeniz; Mehmet Erdogan; Ayhan Zengi; Zuhal Eroglu; Sadik Tamsel; Murat Olukman; Fusun Saygili; Candeger Yilmaz
- Book ID
- 107571464
- Publisher
- Springer
- Year
- 2010
- Tongue
- English
- Weight
- 222 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0969-711X
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## Abstract ## Background Poor glycaemic control, hypertension and duration of diabetes are risk factors for the development of diabetic nephropathy, but there may be genetic factors. Recently, a common C to T mutation at nucleotide position 677 of the MTHFR gene (MTHFR677C > T) has been reported
## 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 communityβbased Japanese population. ## Study Design: N