Kark, R A <br/><br/>
Multiple genotypes, multiple phenotypes, and partial defects.  [electronic resource] 

 -  Muscle & nerve   
 - 31-40 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review 
<br/><br/><label>ISSN: </label>0148-639X 
<br/><br/><label>Standard No.: </label>10.1002/mus.880040107  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anemia, Hemolytic, Congenital--genetics<br/>Arylsulfatases--deficiency<br/>Female<br/>Genetic Variation<br/>Genotype<br/>Glucosephosphate Dehydrogenase Deficiency--genetics<br/>Glycogen Storage Disease Type V--genetics<br/>Humans<br/>Hyperlipoproteinemia Type II--genetics<br/>Male<br/>Models, Genetic<br/>Muscular Atrophy--genetics<br/>Neuromuscular Diseases--genetics<br/>Phenotype<br/>Porphyrias--genetics<br/>Pyruvate Kinase--deficiency<br/>Tay-Sachs Disease--genetics