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Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis Cover

Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis

Endocrine Regulations
Volume 54 (2020): Issue 3 (July 2020)
By: ,  ,  ,  ,   and    
Open Access
|Aug 2020
Articles in this issue
DOI: https://doi.org/10.2478/enr-2020-0025 | Journal eISSN: 1336-0329 | Journal ISSN: 1210-0668
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Language: English
Page range: 227 - 229
Published on: Aug 27, 2020
Published by: Slovak Academy of Sciences, Institute of Experimental Endocrinology
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year
Keywords:
aldosterone,
CYP11B2 gene,
hyponatremia,
hyperkalemia,
metabolic acidosis,
faltering growth
Related subjects:
Life sciences,
Molecular biology,
Neurobiology,
Medicine,
Basic medical science,
Basic medical science, other,
Clinical medicine,
Internal medicine,
Endocrinology, diabetology

© 2020 Stayroula Papailiou, Elpis Athina Vlachopapadopoulou, Amalia Sertedaki, Despoina Maritsi, Nikolaos Syggelos, Angeliki Syggelou, published by Slovak Academy of Sciences, Institute of Experimental Endocrinology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Volume 54 (2020): Issue 3 (July 2020)
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