van der Put, N M <br/><br/>
Decreased methylene tetrahydrofolate reductase activity due to the 677C-->T mutation in families with spina bifida offspring.  [electronic resource] 

 -  Journal of molecular medicine (Berlin, Germany)  Nov 1996 
 - 691-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0946-2716 
<br/><br/><label>Standard No.: </label>10.1007/s001090050073  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>5,10-Methylenetetrahydrofolate Reductase (FADH2)<br/>Adult<br/>Aged<br/>Child<br/>Cysteine--blood<br/>Female<br/>Folic Acid--blood<br/>Genetic Linkage<br/>Genotype<br/>Homocysteine--blood<br/>Homozygote<br/>Humans<br/>Lod Score<br/>Lymphocytes--enzymology<br/>Male<br/>Methylenetetrahydrofolate Reductase (NADPH2)<br/>Middle Aged<br/>Netherlands<br/>Oxidoreductases--deficiency<br/>Point Mutation--genetics<br/>Risk Factors<br/>Spinal Dysraphism--epidemiology<br/>Vitamin B 12--blood