Mutations inCYP11B1 gene: Phenotype-genotype correlations
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference25 articles.
1. Congenital adrenal hyperplasia due to 11 β-hydroxylase deficiency in Saudi Arabia: clinical and biochemical characteristics
2. Cloning of cDNA encoding steroid 11 beta-hydroxylase (P450c11).
3. The CpG dinucleotide and human genetic disease
4. The Product of the CYP11B2 Gene Is Required for Aldosterone Biosynthesis in the Human Adrenal Cortex
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