Search Results - Vyletal, P.
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Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone by Bleyer, Anthony J. (Author) , Zivná, M. (Author) , Hulková, H. (Author) , Hodanová, K. (Author) , Vyletal, P. (Author) , Sikora, J. (Author) , Zivný, J. (Author) , Sovová, J. (Author) , Hart, T. C. (Author) , Adams, J. N. (Author) , Elleder, M. (Author) , Kapp, Katharina (Author) , Haws, R. (Author) , Cornell, L. D. (Author) , Kmoch, S. (Author) , Hart, P. S. (Author) ,
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Adult
Amino Acid Sequence
Anemia
Base Sequence
Biopsy
Blood Pressure
Cell Line
Child
Chronic Disease
Chymosin
Cytoplasm
DNA Mutational Analysis
Endoplasmic Reticulum
Enzyme Precursors
Female
Fludrocortisone
Genes, Dominant
Genetic Predisposition to Disease
Glomerular Filtration Rate
Glycosylation
Heterozygote
Humans
Hyperuricemia
Hypoaldosteronism
Kidney Concentrating Ability
Kidney Diseases
Male
Molecular Sequence Data
Mutation
Pedigree