Bassi, M T <br/><br/>
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America.  [electronic resource] 

 -  Human genetics  Jan 2001 
 - 51-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/s004390000440  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Albinism, Ocular--genetics<br/>DNA Mutational Analysis<br/>Europe<br/>Eye Proteins--genetics<br/>Humans<br/>Membrane Glycoproteins--genetics<br/>Mutation<br/>North America<br/>Sequence Deletion