Geisel, J <br/><br/>
Genetic defects as important factors for moderate hyperhomocysteinemia.  [electronic resource] 

 -  Clinical chemistry and laboratory medicine  Aug 2001 
 - 698-704 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1434-6621 
<br/><br/><label>Standard No.: </label>10.1515/CCLM.2001.115  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase--genetics<br/>Adult<br/>Age Factors<br/>Aged<br/>Aged, 80 and over<br/>Cystathionine--blood<br/>DNA Mutational Analysis<br/>Female<br/>Ferredoxin-NADP Reductase--genetics<br/>Folic Acid--blood<br/>Genotype<br/>Homocysteine--blood<br/>Humans<br/>Hyperhomocysteinemia--genetics<br/>Male<br/>Methylenetetrahydrofolate Reductase (NADPH2)<br/>Methylmalonic Acid--blood<br/>Middle Aged<br/>Mutation<br/>Oxidoreductases Acting on CH-NH Group Donors--genetics<br/>Protein Binding<br/>Risk Factors<br/>Sex Factors<br/>Vitamin B 12--blood<br/>Vitamin B 6--blood