Abid, Fatima <br/><br/>
CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutation.  [electronic resource] 

 -  Clinical chemistry and laboratory medicine  2008 
 - 1707-13 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1434-6621 
<br/><br/><label>Standard No.: </label>10.1515/CCLM.2008.339  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Hyperplasia, Congenital--genetics<br/>Child, Preschool<br/>Female<br/>Genotype<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Morocco<br/>Mutation<br/>Steroid 21-Hydroxylase--genetics