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Anemia
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In frame deletion of glycin 390 in coproporphyrinogen oxidase gene as a cause of hereditary coproporphyria
Publication
5 people
Abstract
molecular biology, hereditary coproporphyria, mutation
People
person
prof. MUDr. Jiří Zeman DrSc.
First Faculty of Medicine
person
MUDr. Robert Rosipal
Faculty of Physical Education and Sport
person
prof. MUDr. Pavel Martásek DrSc.
First Faculty of Medicine
person
J. C. Deybach
Person without faculty affiliation
person
Eva Maloňová
Person without faculty affiliation
