Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia.

Tekijä Engbersen, A M, Franken, D G, Boers, G H, Stevens, E M, Trijbels, F J, Blom, H J
Julkaistu 1995

Defective cystathionine beta-synthase regulation by S-adenosylmethionine in a partially pyridoxine responsive homocystinuria patient.

Tekijä Kluijtmans, L A, Boers, G H, Stevens, E M, Renier, W O, Kraus, J P, Trijbels, F J, van den Heuvel, L P, Blom, H J
Julkaistu 1996

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

Tekijä van der Put, N M, Gabreëls, F, Stevens, E M, Smeitink, J A, Trijbels, F J, Eskes, T K, van den Heuvel, L P, Blom, H J
Julkaistu 1998

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.

Tekijä Kluijtmans, L. A., van den Heuvel, L. P., Boers, G. H., Frosst, P., Stevens, E. M., van Oost, B. A., den Heijer, M., Trijbels, F. J., Rozen, R., Blom, H. J.
Julkaistu 1996