Xu, Jing <br/><br/>
Identification of novel and rare CYP21A2 variants in Chinese patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.  [electronic resource] 

 -  Clinical biochemistry  Jun 2019 
 - 44-49 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1873-2933 
<br/><br/><label>Standard No.: </label>10.1016/j.clinbiochem.2019.04.008  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Hyperplasia, Congenital--genetics<br/>Asian People--genetics<br/>Humans<br/>Mutation<br/>Pseudogenes--genetics<br/>Retrospective Studies