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13. A previously undescribed mutation detected by sequence analysis of CYP21A2 gene in an infant with salt wasting congenital adrenal hyperplasia. Girgis R; Ajamian F; Metcalfe P J Pediatr Endocrinol Metab; 2013; 26(7-8):765-6. PubMed ID: 23907417 [TBL] [Abstract][Full Text] [Related]
14. CYP21A2 gene mutation in South Indian children with congenital adrenal hyperplasia. Ganesh R; Suresh N; Janakiraman L; Ravikumar K Indian Pediatr; 2015 Aug; 52(8):710-1. PubMed ID: 26388637 [No Abstract] [Full Text] [Related]
15. [From gene to disease: adrenogenital syndrome and the CYP21A2 gene]. Claahsen-van der Grinten HL; Hoefsloot LH Ned Tijdschr Geneeskd; 2007 May; 151(21):1174-7. PubMed ID: 17557757 [TBL] [Abstract][Full Text] [Related]