Disease: Lipoid congenital adrenal hyperplasia
- A Novel Intronic Pathogenic Variant in <em>STAR</em> With a Dominant Negative Mechanism Causes Attenuated Lipoid Congenital Adrenal Hyperplasia
- A Novel Intronic Pathogenic Variant in STAR With a Dominant Negative Mechanism Causes Attenuated Lipoid Congenital Adrenal Hyperplasia
- A novel variant of the <em>STAR</em> gene: nonclassical presentation from Turkey
- Aldosterone signaling defect in young infants: single-center report and review
- Characterization of Two Novel Variants of the Steroidogenic Acute Regulatory Protein Identified in a Girl with Classic Lipoid Congenital Adrenal Hyperplasia
- Chronic social defeat stress causes retinal vascular dysfunction
- Clinical and functional analyses of the novel STAR c.558C>A in a patient with classic lipoid congenital adrenal hyperplasia
- Clinical and functional analyses of the novel STAR c.558C>A in a patient with classic lipoid congenital adrenal hyperplasia
- Clinical and Genetic Characteristics of Patients with Common and Rare Types of Congenital Adrenal Hyperplasia: Novel Variants in <em>STAR</em> and <em>CYP17A1</em>
- Clinical and molecular characterization of thirty Chinese patients with congenital lipoid adrenal hyperplasia
- Clinical and StAR genetic characteristics of 33 children with congenital lipoid adrenal hyperplasia
- Clinical applications of genetic analysis and liquid chromatography tandem-mass spectrometry in rare types of congenital adrenal hyperplasia
- Clinical characteristics of a male child with non-classic lipoid congenital adrenal hyperplasia and literature review
- Clinical spectrum of human STAR variants and their genotype-phenotype correlation
- Congenital lipoid adrenal hyperplasia in a Saudi infant
- Congenital lipoid adrenal hyperplasia with Graves' disease: A case report
- Disorders of Sex Development of Adrenal Origin
- Lipoid Congenital Adrenal Hyperplasia With a Novel StAR Gene Mutation
- New molecular insights into the A218V variant impact on the steroidogenic acute regulatory protein (STAR) associated with 46, XY disorders of sexual development
- Noninvasive prenatal test of single-gene disorders by linked-read direct haplotyping: application in various diseases
- Novel <em>STAR</em> Gene Variant of Congenital Lipoid Adrenal Hyperplasia With Testicular Adrenal Rests
- Novel STAR gene variant in a patient with classic lipoid congenital adrenal hyperplasia and combined pituitary hormone deficiency
- Role of Constitutive STAR in Leydig Cells
- STAR gene mutation in a patient with congenital lipoid adrenal hyperplasia
- Steroidogenic acute regulatory protein (STAR) deficiency: Our experience and systematic review for phenotype-genotype correlation
- The uncommon forms of congenital adrenal hyperplasia