Author

Dorothea Götze

Institutions: Heidelberg University, University Hospital Heidelberg

Observed institutions: Heidelberg University, University Hospital Heidelberg, Christian-Albrechts-Universität zu Kiel, University Hospital Schleswig-Holstein

OpenAlex ID: A5002807679

Congenital Adrenal Hyperplasia Due to 11-Hydroxylase Deficiency: Functional Characterization of Two Novel Point Mutations and a Three-Base Pair Deletion in theCYP11B1Gene

2005 · Nils Krone, Felix G. Riepe, et al. · The Journal of Clinical Endocrinology & Metabolism · 58

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The serotonin receptor 3E variant is a risk factor for female IBS-D

2022 · Nikola Fritz, Sabrina Berens, et al. · Journal of Molecular Medicine · 12

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The alternative serotonin transporter promoter P2 impacts gene function in females with irritable bowel syndrome

2021 · Sandra Mohr, Nikola Fritz, et al. · Journal of Cellular and Molecular Medicine · 11

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Funktionelle Charakterisierung 8 neuer Mutationen des CYP11B2 Gens

2012 · Dorothea Götze · Multimedialen Archiv und Publikationsserver der Christian-Albrechts-Universität zu Kiel (Christian-Albrechts-Universität zu Kiel)

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Works count: 4

Citation count: 81

H-index: 3

I10-index: 3