Publications
- cblE type of homocystinuria due to methionine synthase reductase deficiency: Functional correction by minigene expression2005 | First Faculty of Medicine
- cblE type of homocystinuria due to methionine synthase reductase deficiency: Functional correction by minigene expresion2005 | Faculty of Physical Education and Sport
- cblE type of homocystinuria due to methionine synthase reductase deficiency: Functional correction by minigene expression2005 | Faculty of Physical Education and Sport
- CblE type of homocystinuria due to methionine synthase reductase deficiency: Clinical and molecular studies and prenatal diagnosis in two families2002 | Faculty of Physical Education and Sport
- Molecular and functional studies in patients with the cblE type of homocystinuriaPublication without faculty affiliation
- Single-nucleotide polymorphisms in genes relating to homocysteine metabolism: how applicable are public SNP databases to a typical European population?2005 | First Faculty of Medicine
- The cblD defect causes either isolated or combined deficiency of methylcobalamin and adenosylcobalamin synthesis.2004 | First Faculty of Medicine
- The cblD defect causes either isolated or combined deficiency of methylcobalamin and adenosylcobalamin synthesis2004 | Faculty of Physical Education and Sport
- CblE type of homocystinuria: Mild clinical phenotype in two patients homozygous for a novel mutation in the MTRR gene2003 | First Faculty of Medicine
- CblE type of homocystinuria: Mild clinical phenotype in two patients homozygous for a novel mutation in the MTRR gene2003 | Faculty of Physical Education and Sport
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