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Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis
Title Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis Author info Stayroula Papailiou ... [et al.] Co-authors Papailiou Stayroula
Note Bibliogr. odkazy. - Res. angl. Sign. C 1685 Source Endocrine regulations. - ISSN 1210-0668. - Bratislava : Institute of Experimental Endocrinology , 2020 . - Vol. 54, no. 3 (2020), s. 227-229 MeSH Subject cytochróm P-450 CYP11B2 : deficit : genetika : novorodenec
mutácia
príznaky a symptómy
diagnostika diferenciálna
farmakoterapia
novorodenec
Subj. Headings deficiencia aldosterónsyntázy typ II * mutácia génu CYP11B2 - variant c.554C>T (p.T185I) * kazuistika Language English Country Slovak Republic Document kind Rozpis článkov z periodík Database ARTICLES 
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Number of the records: 1