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Article

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

Hormones (Athens, Greece) - 1 Apr 2016

Yurekli Banu Sarer, Kutbay Nilufer Ozdemir, Onay Huseyin, Simsir Ilgin Yildirim, Kocabas Gokcen Unal, Erdogan Mehmet, Cetinkalp Sevki, Ozgen Gokhan, Saygili Fusun

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Share to Adrenal Hyperplasia, Congenital
Share to DNA Mutational Analysis
Share to Heterozygote

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Hypokalemia

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Share to Steroid 11-beta-Hydroxylase

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Identifiers

PMID: 27376433
DOI: 10.14310/horm.2002.1654

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A novel CYP11B1 mutation in a Turkish patient with 11β-hydroxylase deficiency: An association with the severe hypokalemia leading to rhabdomyolysis.PMID 27376433Read ↗

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