Rees, Matthew G <br/><br/>
Correlation of rare coding variants in the gene encoding human glucokinase regulatory protein with phenotypic, cellular, and kinetic outcomes.  [electronic resource] 

 -  The Journal of clinical investigation  Jan 2012 
 - 205-17 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1558-8238 
<br/><br/><label>Standard No.: </label>10.1172/JCI46425  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Active Transport, Cell Nucleus<br/>Adaptor Proteins, Signal Transducing--genetics<br/>Aged<br/>Amino Acid Substitution<br/>Codon, Nonsense<br/>Cohort Studies<br/>Evolution, Molecular<br/>Exons<br/>Female<br/>Frameshift Mutation<br/>Genetic Variation<br/>Glucokinase--metabolism<br/>HeLa Cells<br/>Humans<br/>Kinetics<br/>Male<br/>Middle Aged<br/>Mutation, Missense<br/>Phenotype<br/>Polymorphism, Single Nucleotide<br/>Recombinant Proteins--genetics<br/>Triglycerides--blood