Ali, Shahbaz <br/><br/>
Phenotypic variability associated with the D226N allele of IMPDH1.  [electronic resource] 

 -  Ophthalmology  Feb 2015 
 - 429-31 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1549-4713 
<br/><br/><label>Standard No.: </label>10.1016/j.ophtha.2014.07.057  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Alleles<br/>Child<br/>Consanguinity<br/>Electroretinography<br/>Female<br/>Genetic Linkage<br/>Humans<br/>IMP Dehydrogenase--genetics<br/>Infant<br/>Male<br/>Middle Aged<br/>Pedigree<br/>Phenotype<br/>Photic Stimulation<br/>Retinitis Pigmentosa--diagnosis<br/>Young Adult