Millá, Elena <br/><br/>
Survey of familial glaucoma shows a high incidence of cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) mutations in non-consanguineous congenital forms in a Spanish population.  [electronic resource] 

 -  Molecular vision  2013 
 - 1707-22 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1090-0535 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anterior Eye Segment--abnormalities<br/>Aryl Hydrocarbon Hydroxylases--genetics<br/>Consanguinity<br/>Cytochrome P-450 CYP1B1<br/>Cytoskeletal Proteins--genetics<br/>DNA Mutational Analysis<br/>Eye Abnormalities--enzymology<br/>Eye Diseases, Hereditary<br/>Eye Proteins--genetics<br/>Family<br/>Female<br/>Genetic Association Studies<br/>Genetic Predisposition to Disease<br/>Glaucoma--congenital<br/>Glycoproteins--genetics<br/>Health Surveys<br/>Heterozygote<br/>Humans<br/>Incidence<br/>Male<br/>Mutation--genetics<br/>Pedigree<br/>Spain--epidemiology