Scriver, C R <br/><br/>
Phenylketonuria and other phenylalanine hydroxylation mutants in man.  [electronic resource] 

 -  Annual review of genetics  1980 
 - 179-202 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>0066-4197 
<br/><br/><label>Standard No.: </label>10.1146/annurev.ge.14.120180.001143  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Amino Acid Metabolism, Inborn Errors--diagnosis<br/>Animals<br/>Biopterins--analogs & derivatives<br/>Dihydropteridine Reductase--genetics<br/>Female<br/>Fetal Diseases--etiology<br/>Gene Frequency<br/>Genetic Carrier Screening<br/>Heterozygote<br/>Humans<br/>Hydroxylation<br/>Phenylalanine--metabolism<br/>Phenylalanine Hydroxylase--deficiency<br/>Phenylketonurias--diet therapy<br/>Pregnancy<br/>Pregnancy Complications<br/>Rats