Defects in the HSD11 gene encoding 11β-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency

Heli Nikkilä, Grace M. Tannin, Maria I. New, Norman F. Taylor, George Kalaitzoglou, Carl Monder, Perrin C. White

Research output: Contribution to journalArticle

Original languageEnglish (US)
Pages (from-to)344
Number of pages1
JournalPediatric Nephrology
Volume8
Issue number3
DOIs
StatePublished - Jun 1994

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11-beta-Hydroxysteroid Dehydrogenases
Genes
Apparent mineralocorticoid excess

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Nephrology

Cite this

Defects in the HSD11 gene encoding 11β-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiency. / Nikkilä, Heli; Tannin, Grace M.; New, Maria I.; Taylor, Norman F.; Kalaitzoglou, George; Monder, Carl; White, Perrin C.

In: Pediatric Nephrology, Vol. 8, No. 3, 06.1994, p. 344.

Research output: Contribution to journalArticle

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