Publication | Closed Access
Association of methylenetetrahydrofolate reductase A1298C polymorphism but not of C677T with multiple sclerosis in Tunisian patients
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Citations
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References
2013
Year
Genetic DisorderMedicineGeneticsInherited Metabolic DiseaseGenetic EpidemiologyHuman PolymorphismPathologyTunisian PatientsMultiple SclerosisPublic HealthMolecular DiagnosticsImmune-related Gene PolymorphismClinical Genetics
| Year | Citations | |
|---|---|---|
2011 | 9.7K | |
A Second Common Mutation in the Methylenetetrahydrofolate Reductase Gene: An Additional Risk Factor for Neural-Tube Defects? N.M.J. van der Put, F. Gabreëls, E M Stevens, The American Journal of Human Genetics Developmental BiologySecond Common MutationNeural-tube DefectsGenetic DisorderMendelian Disorder | 1998 | 1.6K |
1998 | 1.3K | |
2017 | 1.1K | |
2000 | 781 | |
2008 | 468 | |
2009 | 272 | |
1991 | 234 | |
2006 | 106 | |
2003 | 84 |
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