Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria | Charles Explorer

Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria

Publikace na Fakulta tělesné výchovy a sportu |

2002

Abstrakt

Hereditary coproporphyria, porphyria cutanea tarda, gene mutation

Osoba