Gravel, R A <br/><br/>
Mutations participating in interallelic complementation in propionic acidemia.  [electronic resource] 

 -  American journal of human genetics  Jul 1994 
 - 51-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Amino Acid Metabolism, Inborn Errors--genetics<br/>Amino Acid Sequence<br/>Base Sequence<br/>Binding Sites<br/>Carboxy-Lyases--chemistry<br/>Cell Line<br/>Conserved Sequence<br/>DNA Mutational Analysis<br/>Frameshift Mutation<br/>Genetic Complementation Test<br/>Humans<br/>Methylmalonyl-CoA Decarboxylase<br/>Molecular Sequence Data<br/>Mutagenesis, Insertional<br/>Mutation<br/>Point Mutation<br/>Propionates--blood<br/>Propionibacterium--genetics<br/>Sequence Deletion<br/>Sequence Homology, Amino Acid<br/>Suppression, Genetic