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CAH due to 11β-hydroxylase deficiency - same same but different!
CAH due to 11β-hydroxylase deficiency - same same but different!
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BORIS DOI
10.48620/92096
Publisher DOI
10.1210/clinem/dgaf576
PubMed ID
41145228
Date of Publication
2025-10-27
Publication Type
Article
Subject(s)
600 Technology
>
610 Medicine & health
Keyword(s)
11β-hydroxylase deficiency
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•
CYP11B1
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congenital adrenal hyperplasia
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genetics
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phenotype-genotype
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splicing
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Language(s)
en
Contributor(s)
du Toit, Therina
Clinic of Nephrology and Hypertension
Flück, Christa
Department of Paediatrics
Department for BioMedical Research, Forschungsgruppe Endokrinologie / Diabetologie / Metabolik (Pädiatrie)
Additional Credits
Clinic of Nephrology and Hypertension
Department of Paediatrics
Series
The Journal of Clinical Endocrinology & Metabolism
Publisher
Oxford University Press
ISSN
1945-7197
0021-972X
Access(Rights)
embargo
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