Author:
Chen Hong,Yuan Ke,Zhang Bingtao,Jia Zexiao,Chen Chun,Zhu Yilin,Sun Yaping,Zhou Hui,Huang Wendong,Liang Li,Yan Qingfeng,Wang Chunlin
Subject
Genetics (clinical),Genetics,Molecular Medicine
Reference24 articles.
1. Mutational analysis of rare subtypes of congenital adrenal hyperplasia in a highly inbred population;Alswailem;Mol. Cell Endocrinol.,2018
2. Hypokalemic rhabdomyolysis in a child with 11-hydroxylase deficiency;Atabek;J. Pediatr. Endocrinol. Metab.,2008
3. The genetics, pathophysiology, and management of human deficiencies of P450c17;Auchus;Endocrinol. Metab. Clin. North Am.,2001
4. Steroid 17-hydroxylase and 17,20-lyase deficiencies, genetic and pharmacologic;Auchus;J. Steroid Biochem. Mol. Biol.,2017
5. 17Alpha-hydroxylase/17,20-lyase deficiency as a model to study enzymatic activity regulation: role of phosphorylation;Biason-Lauber;J. Clin. Endocrinol. Metab.,2000
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