Congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

By Kathleen Glatt, D. Garzon, J. Popovic. Journal for Specialists in Pediatric Nursing, 2005

803 citations recorded by the source corpus.

Subfields: Clinical Biochemistry, Endocrinology, Diabetes and Metabolism, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/f3291cb1b8a8ae214c83b499dc7dcad645a188a8

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1. Raffaella Ida Rumiati
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Citations in the corpus

• Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline. (2010, neutral): “The most common form of CAH is caused by mutations in CYP21A2, the gene encoding the adrenal steroid 21-hydroxylase enzyme (P450c21) (5,6).”
• Hardwired for Sexism? Approaches to Sex/Gender in Neuroscience (2012, background): “, disrupted synthesis of mood-regulating hormones; short stature; and high rates of obesity, cystic acne, hirsutism, and male-pattern baldness) [70–72].”