Correction: Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations.

Autor: Menabò S; Program of Pediatric Endocrinology, Pediatric Unit, Department of Medical and Surgical Sciences; Azienda Policlinico S. Orsola Malpighi, University of Bologna, Bologna, Italy., Polat S; Medical Genetics Department, Erciyes University, Kayseri, Turkey., Baldazzi L; Program of Pediatric Endocrinology, Pediatric Unit, Department of Medical and Surgical Sciences; Azienda Policlinico S. Orsola Malpighi, University of Bologna, Bologna, Italy., Kulle AE; Division of Pediatric Endocrinology, Department of Pediatrics, University Hospital, Schleswig-Holstein, Campus Kiel, Kiel, Germany., Holterhus PM; Division of Pediatric Endocrinology, Department of Pediatrics, University Hospital, Schleswig-Holstein, Campus Kiel, Kiel, Germany., Grötzinger J; Biochemical Institute, Christian-Albrecht University of Kiel, Kiel, Germany., Fanelli F; Endocrinology Unit-Department of Medical and Surgical Sciences, Center for Applied Biomedical Research (CRBA), Bologna, Italy., Balsamo A; Program of Pediatric Endocrinology, Pediatric Unit, Department of Medical and Surgical Sciences; Azienda Policlinico S. Orsola Malpighi, University of Bologna, Bologna, Italy. antonio.balsamo@unibo.it., Riepe FG; Division of Pediatric Endocrinology, Department of Pediatrics, University Hospital, Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Jazyk: angličtina
Zdroj: European journal of human genetics : EJHG [Eur J Hum Genet] 2020 May; Vol. 28 (5), pp. 692.
DOI: 10.1038/s41431-020-0587-y
Abstrakt: An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Databáze: MEDLINE
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