![]() |
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
Ann Pediatr Endocrinol Metab. 2018;23(3):158-161. Published online 2018 Sep 28 DOI: https://doi.org/10.6065/apem.2018.23.3.158
|
Citations to this article as recorded by
21-hydroxylase deficiency and fertility
M. M. Amiraslanova, I. V. Kuznetsova
Medical alphabet.2020; (4): 16. CrossRef
|