Dahri, Saloua <br/><br/>
Mutation analysis of phenylketonuria patients from Morocco: high prevalence of mutation G352fsdelG and detection of a novel mutation p.K85X.  [electronic resource] 

 -  Clinical biochemistry  Jan 2010 
 - 76-81 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1873-2933 
<br/><br/><label>Standard No.: </label>10.1016/j.clinbiochem.2009.09.018  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>DNA Mutational Analysis<br/>Electrophoresis, Polyacrylamide Gel<br/>Genotype<br/>Heterozygote<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Morocco--epidemiology<br/>Mutation<br/>Phenotype<br/>Phenylalanine Hydroxylase--genetics<br/>Phenylketonurias--epidemiology<br/>Spain