Heil, S G <br/><br/>
Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects?  [electronic resource] 

 -  Molecular genetics and metabolism  Jun 2001 
 - 164-72 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1096-7192 
<br/><br/><label>Standard No.: </label>10.1006/mgme.2001.3175  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Alleles<br/>Base Sequence<br/>Child<br/>Cytosol--enzymology<br/>DNA Mutational Analysis<br/>DNA, Complementary--chemistry<br/>Female<br/>Folic Acid--blood<br/>Genotype<br/>Glycine Hydroxymethyltransferase--genetics<br/>Humans<br/>Mitochondria--enzymology<br/>Mutation<br/>Neural Tube Defects--enzymology<br/>Polymorphism, Genetic<br/>Polymorphism, Single-Stranded Conformational<br/>Sequence Deletion