Publications
- Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria2005 | Faculty of Physical Education and Sport
- Congenital erythropoietic porphyria (Gunther disease)2001 | Faculty of Physical Education and Sport
- Human coproporphyrinogen oxidase: biochemical characterization of wild-type enzyme and its naturally occurring R331W mutant form2001 | Faculty of Physical Education and Sport
- In frame deletion of glycin 390 in coproporphyrinogen oxidase gene as a cause of hereditary coproporphyria2001 | Faculty of Physical Education and Sport
- Menke's disease and respiratory chain abnormalities2001 | Faculty of Physical Education and Sport
- Hereditary copropofphyria.2000 | Faculty of Physical Education and Sport
- Porphyria with clinic manifestation in child age.2000 | Faculty of Physical Education and Sport
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