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Author:(Salman KIRMANI)

1.Compound heterozygosity for a whole gene deletion and p.R124C mutation in CYP21A2 causing nonclassic congenital adrenal hyperplasia.

Hamza NASIR ; Syed Ibaad ALI ; Naeem HAQUE ; Stefan K GREBE ; Salman KIRMANI

Annals of Pediatric Endocrinology & Metabolism 2018;23(3):158-161

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