Livedo vasculopathy associated with methylenetetrahydrofolate reductase C677T homozygosity
✍ Scribed by Mari KISHIBE; Shigetsuna KOMATSU; Akemi ISHIDA-YAMAMOTO; Hajime IIZUKA
- Book ID
- 108578104
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- French
- Weight
- 270 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0385-2407
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## Abstract Different lines of evidence indicate that methylenetetrahydrofolate reductase (__MTHFR__) functional gene polymorphisms, causative in aberrant folate–homocysteine metabolism, are associated with increased vulnerability to several heritable developmental disorders. Opposing views are exp
## 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