Associated Papers
Analysis of novel heterozygous mutations in the CYP11B2 gene causing congenital aldosterone synthase deficiency and literature review.
Miao H et al.
Steroids, 2019
Molecular mechanisms of disease-causing missense mutations.
Stefl S et al.
Journal of Molecular Biology, 2013
Cytochromes p450: roles in diseases.
Pikuleva IA et al.
The Journal of Biological Chemistry, 2013
Two novel mutations of the CYP11B2 gene in a Japanese patient with aldosterone deficiency type 1.
Kondo E et al.
Endocrine Journal, 2013
Five novel mutations in CYP11B2 gene detected in patients with aldosterone synthase deficiency type I: Functional characterization and structural analyses.
Nguyen HH et al.
Molecular Genetics and Metabolism, 2010
Select a paper to view details