Author:
Khajuria Ragini,Walia Rama,Bhansali Anil,Prasad Rajendra
Funder
Science and Engineering Research Board, New Delhi
Indian council of medical research for ICMR-JRF and SRF
Subject
General Medicine,Biochemistry
Reference26 articles.
1. The clinical and biochemical spectrum of congenital adrenal hyperplasia secondary to 21- hydroxylase deficiency;Huynh;Clin. Biochem. Rev.,2009
2. Clinical and molecular review of atypical congenital adrenal hyperplasia;Sahakitrungruang;Annals of Pediatric Endocrinology & Metabolism,2015
3. p.H282N and p.Y191H: 2 novel CYP21A2 mutations in Italian congenital adrenal hyperplasia patients;Concolino;Metab., Clin. Exp.,2012
4. In vitro functional studies of rare CYP21A2 mutations and establishment of an activity gradient for nonclassic mutations improve phenotype predictions in congenital adrenal hyperplasia;Barbaro;Clin. Endocrinol.,2015
5. Functional Studies of p.R132C, p.R149C, p.M283V, p.E431K, and a Novel c.652-2A.G Mutations of the CYP21A2 Gene;Taboas;PLoS One,2014
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献