Riepe, Felix G <br/><br/>
Congenital adrenal hyperplasia: the molecular basis of 21-hydroxylase deficiency in H-2(aw18) mice.  [electronic resource] 

 -  Endocrinology  Jun 2005 
 - 2563-74 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0013-7227 
<br/><br/><label>Standard No.: </label>10.1210/en.2004-1563  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Hyperplasia, Congenital--genetics<br/>Amino Acid Sequence<br/>Animals<br/>Base Sequence<br/>Blotting, Southern<br/>Codon, Nonsense<br/>Crossing Over, Genetic<br/>Disease Models, Animal<br/>Gene Expression Regulation, Developmental<br/>Gene Expression Regulation, Enzymologic<br/>Genotype<br/>Mice<br/>Mice, Inbred C57BL<br/>Mice, Mutant Strains<br/>Microsatellite Repeats<br/>Molecular Sequence Data<br/>Mutagenesis, Site-Directed<br/>Mutation, Missense<br/>Polymerase Chain Reaction<br/>Protein Structure, Tertiary<br/>Pseudogenes--genetics<br/>RNA, Messenger--analysis<br/>Steroid 21-Hydroxylase--chemistry<br/>Structure-Activity Relationship