Buraczynska, M <br/><br/>
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa.  [electronic resource] 

 -  American journal of human genetics  Dec 1997 
 - 1287-92 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>0002-9297 
<br/><br/><label>Standard No.: </label>10.1086/301646  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Carrier Proteins--genetics<br/>Cohort Studies<br/>DNA Mutational Analysis<br/>Exons--genetics<br/>Eye Proteins<br/>Humans<br/>Male<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Polymorphism, Genetic<br/>RNA Splicing<br/>Retinitis Pigmentosa--genetics<br/>Sequence Deletion<br/>X Chromosome--genetics