Publikace
- cblE type of homocystinuria due to methionine synthase reductase deficiency: Functional correction by minigene expression2005 | 1. lékařská fakulta
- Single-nucleotide polymorphisms in genes relating to homocysteine metabolism: how applicable are public SNP databases to a typical European population?2005 | 1. lékařská fakulta
- cblE type of homocystinuria due to methionine synthase reductase deficiency: Functional correction by minigene expresion2005 | Fakulta tělesné výchovy a sportu
- cblE type of homocystinuria due to methionine synthase reductase deficiency: Functional correction by minigene expression2005 | Fakulta tělesné výchovy a sportu
- The cblD defect causes either isolated or combined deficiency of methylcobalamin and adenosylcobalamin synthesis.2004 | 1. lékařská fakulta
- The cblD defect causes either isolated or combined deficiency of methylcobalamin and adenosylcobalamin synthesis2004 | Fakulta tělesné výchovy a sportu
- CblE type of homocystinuria: Mild clinical phenotype in two patients homozygous for a novel mutation in the MTRR gene2003 | 1. lékařská fakulta
- CblE type of homocystinuria: Mild clinical phenotype in two patients homozygous for a novel mutation in the MTRR gene2003 | Fakulta tělesné výchovy a sportu
- CblE type of homocystinuria due to methionine synthase reductase deficiency: Clinical and molecular studies and prenatal diagnosis in two families2002 | Fakulta tělesné výchovy a sportu
- Molecular and functional studies in patients with the cblE type of homocystinuriaPublikace bez příslušnosti k fakultě
Loading network view...