Increased prevalence of heterozygous 21-OH germline mutations in patients with adrenal incidentalomas

Author:

Baumgartner-Parzer S. M.,Pauschenwein S.,Waldhäusl W.,Pölzler K.,Nowotny P.,Vierhapper H.

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Reference25 articles.

1. Mutational spectrum of the steroid 21-hydroxylase gene in Austria: Identification of a novel missense mutation;Baumgartner-Parzer;Journal of Clinical Endocrinology and Metabolism,2001

2. Steroid 21-hydroxylase mutations and 21-hydroxylase messenger ribonucleic acid expression in human adrenocortical tumors;Beuschlein;Journal of Clinical Endocrinology and Metabolism,1998

3. Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease;Blanchong;Journal of Experimental Medicine,2000

4. Adrenal mass;Cook;Endocrinology and Metabolism Clinics of North America,1997

5. Genotyping of CYP21, linked chromosome 6p Markers, and a sex-specific gene in neonatal screening for congenital adrenal hyperplasia;Fitness;Journal of Clinical Endocrinology and Metabolism,1999

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