The frequency of Raynaud’s phenomenon in patients with methylenetetrahydrofolate reductase gene mutation and hyperhomocysteinemia

פריטים דומים

• Intermediate hyperhomocysteinemia resulting from compound heterozygosity of methylenetetrahydrofolate reductase mutations.
  מאת: Kang, S S, et al.
  יצא לאור: (1991)
• Cystathionine β-synthase and methylenetetrahydrofolate reductase mutations in Mexican individuals with hyperhomocysteinemia
  מאת: Figueroa-Torres, Anahi Guadalupe, et al.
  יצא לאור: (2020)
• The frequency of the methylenetetrahydrofolate reductase-gene mutation varies with age in the normal population.
  מאת: Matsushita, S, et al.
  יצא לאור: (1997)
• Combined choroidal neovascularization and hypopituitarism in a patient with homozygous mutation in methylenetetrahydrofolate reductase gene
  מאת: Aydogdu, Aydogan, et al.
  יצא לאור: (2014)
• Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency.
  מאת: Goyette, P, et al.
  יצא לאור: (1995)