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| Relationship between Methylenetetrahydrofolate Reductase C677T Homozygous Mutation and Cerebral Small Vessel Disease Subtypes |
| Jung Hoon Han, Han Jun Kim, Kyungmi Oh, Chi Kyung Kim |
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J Neurosonol Neuroimag. 2021;13(2):64-70. Published online December 29, 2021 DOI: https://doi.org/10.31728/jnn.2021.00106 |
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Relationship between Methylenetetrahydrofolate Reductase C677T Homozygous Mutation and Cerebral Small Vessel Disease Subtypes Journal of Neurosonology and Neuroimaging. 2021;13(2):64-70  Methylenetetrahydrofolate reductase gene C677T mutation is related to the defects in the internal elastic lamina of the artery wall European Journal of Clinical Investigation. 2002;32(12):869-873 The methylenetetrahydrofolate reductase gene C677T polymorphism in patients with homozygous sickle cell disease and stroke British Journal of Haematology. 1999;107(3):569-571 The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine American Journal of Medical Genetics. 2000;96(6):762-764 Interaction between cerebral small vessel disease and neurodegenerative changes Cerebral Small Vessel Disease. 2014;298-310 The link between large artery aging and cerebral small vessel disease Cerebral Small Vessel Disease. 2014;92-98 MP-07.01 Relationship Between Genetic Polymorphisms of Methylenetetrahydrofolate Reductase (C677T, A1298C, and G1793A) as Risk Factors for Idiopathic Male Infertility Urology. 2011;78(3):S76 Homozygous methylenetetrahydrofolate reductase C677T mutation in a woman with spinal cord infarction European Journal of Neurology. 2006;13(9):e4-e4 An association between the methylenetetrahydrofolate reductase (MTHFR) C677T mutation and inflammation markers related to cardiovascular disease International Journal of Cardiology. 2005;100(3):409-414 A low prevalence of the C677T mutation in the methylenetetrahydrofolate reductase gene in Asian Indians Clinical Genetics. 2002;61(2):155-159 |
