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Object |
| contentType |
Journal Article|Research Support, Non-U.S. Gov't |
| endingPage |
1051 |
| issn |
0026-0495 |
| issueIdentifier |
8 |
| pageRange |
1047-1051 |
| publicationName |
Metabolism: clinical and experimental |
| startingPage |
1047 |
| bibliographicCitation |
Yoo JH, Hong SB. A common mutation in the methylenetetrahydrofolate reductase gene is a determinant of hyperhomocysteinemia in epileptic patients receiving anticonvulsants. Metabolism. 1999 Aug;48(8):1047–51. doi: 10.1016/s0026-0495(99)90204-4. PMID: 10459572. |
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http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_42c570d9a3d626241fde82721f2ab064 |
| date |
199908 |
| identifier |
https://doi.org/10.1016/s0026-0495%2899%2990204-4
https://pubmed.ncbi.nlm.nih.gov/10459572 |
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http://rdf.ncbi.nlm.nih.gov/pubchem/journal/5782 |
| language |
English |
| source |
https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/ |
| title |
A common mutation in the methylenetetrahydrofolate reductase gene is a determinant of hyperhomocysteinemia in epileptic patients receiving anticonvulsants |
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