O. Šeda
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A Novel Mutation in the FECH Gene in a Czech Family with Erythropoietic Protoporphyria and a Population Study of IVS3-48C Variant Contributing to the Disease
M. S. Farrag, J. Kučerová, L. Šlachtová, O. Šeda, J. Šperl, Pavel Martásek
2015, Vol. 61, Issue 6, pp. 227-232
The following name might also represent this author:
Ondřej Šeda
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Spontaneously Hypertensive Rat Chromosome 2 with Mutant Connexin 50 Triggers Divergent Effects on Metabolic Syndrome Components
Ondřej Šeda, D. Křenová, L. Šedová, L. Kazdová, M. Krupková, B. Chylíková, F. Liška, V. Křen
2017, Vol. 63, Issue 2, pp. 67-77
