A novel CYP11B1 mutation in a Turkish patient with 11 beta-hydroxylase deficiency: An association with the severe hypokalemia leading to rhabdomyolysis

Yurekli, Banu SarerKutbay, Nilufer OzdemirOnay, HuseyinSimsir, Ilgin YildirimKocabas, Gokcen UnalErdogan, MehmetCetinkalp, SevkiOzgen, GokhanSaygili, Fusun2019-10-272019-10-2720161109-3099https://doi.org/10.14310/horm.2002.1654https://hdl.handle.net/11454/52893en10.14310/horm.2002.1654info:eu-repo/semantics/openAccess11-B hydroxylase deficiencyHypokalemiaNovel mutationA novel CYP11B1 mutation in a Turkish patient with 11 beta-hydroxylase deficiency: An association with the severe hypokalemia leading to rhabdomyolysisLetter152300302WOS:00037883390001727376433Q4