Genotype-Phenotype Correlations in Patients with Hereditary Angioedema
Identification of novel CYP21A2 mutations in patients with 21-hydroxylase deficiency
Three novel mutations in brazilians patients with classical form of 21-hydroxylase...
Three novel mutations in cyp21 gene in brazilian patients with the classical form ...
Analysis of alterations in the gene expression and in the enzymatic activity resul...
Investigation of cellular and molecular mechanisms associated with the deficiency ...