Vrzalová, Zuzana <br/><br/>
Identification of CYP21A2 mutant alleles in Czech patients with 21-hydroxylase deficiency.  [electronic resource] 

 -  International journal of molecular medicine  Oct 2010 
 - 595-603 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1791-244X 
<br/><br/><label>Standard No.: </label>10.3892/ijmm_00000504  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Hyperplasia, Congenital--diagnosis<br/>Alleles<br/>Czech Republic<br/>Gene Deletion<br/>Gene Duplication<br/>Genotype<br/>Humans<br/>Mutation<br/>Phenotype<br/>Point Mutation<br/>Steroid 21-Hydroxylase--genetics