Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip

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...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	American journal of medical genetics 1998-11, Vol.80 (3), p.196-198
Hauptverfasser:	Shaw, Gary M., Rozen, Rima, Finnell, Richard H., Todoroff, Karen, Lammer, Edward J.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences birth defects Case-Control Studies Cleft Lip - genetics Cytosine Facial bones, jaws, teeth, parodontium: diseases, semeiology Female Fertilization gene-environment interaction Humans Infant, Newborn Medical sciences Methylenetetrahydrofolate Reductase (NADPH2) Mutation Non tumoral diseases Otorhinolaryngology. Stomatology Oxidoreductases Acting on CH-NH Group Donors - genetics Pregnancy Thymine vitamins Vitamins - pharmacology
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!