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Isolated methylenetetrahydrofolate reductase (MTHFR) gene mutations and pregnancy outcome

✍ Scribed by Hye Heo; Kay O'meara; Kafui Demasio

Book ID
113431472
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
57 KB
Volume
195
Category
Article
ISSN
1097-6868

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## Communicated by Mark Paalman Severe deficiency of methylenetetrahydrofolate reductase (MTHFR) is the most common inborn error of folate metabolism. Patients are characterized by severe hyperhomocysteinemia, homocystinuria and a variety of neurological and vascular problems. Eighteen rare mutatio