Craig, J E <br/><br/>
Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier.  [electronic resource] 

 -  Ophthalmology  Sep 2001 
 - 1607-20 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0161-6420 
<br/><br/><label>Standard No.: </label>10.1016/s0161-6420(01)00654-6  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Codon, Nonsense<br/>Cross-Sectional Studies<br/>Cytoskeletal Proteins<br/>DNA Mutational Analysis<br/>Effect Modifier, Epidemiologic<br/>Eye Proteins--genetics<br/>Female<br/>Genetic Carrier Screening<br/>Genetic Heterogeneity<br/>Glaucoma, Open-Angle--diagnosis<br/>Glutamine<br/>Glycoproteins--genetics<br/>Humans<br/>Intraocular Pressure<br/>Male<br/>Middle Aged<br/>Optic Disk--pathology<br/>Pedigree<br/>Phenotype<br/>Polymorphism, Single-Stranded Conformational<br/>Tasmania--epidemiology<br/>Visual Fields