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Homozygous MTHFR C677T Gene Mutation and Recurrent Stroke in an Infant

✍ Scribed by Anastasia J. Garoufi; Alexia A. Prassouli; Achilleas V. Attilakos; Konstantinos A. Voudris; Eustathia S. Katsarou


Book ID
116824940
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
110 KB
Volume
35
Category
Article
ISSN
0887-8994

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Infant C677T mutation in MTHFR, maternal
✍ Shaw, Gary M.; Rozen, Rima; Finnell, Richard H.; Todoroff, Karen; Lammer, Edward πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 16 KB πŸ‘ 2 views

Studies have reported an association between homozygosity for a variant form of the methylenetetrahydrofolate reductase (MTHFR) gene and risk for neural tube defects. Because of MTHFR's involvement with folate metabolism and evidence that maternal use of a multivitamin with folic acid in early pregn