Shahzadi, Amber <br/><br/>
Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family.  [electronic resource] 

 -  The British journal of ophthalmology  Aug 2010 
 - 1094-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-2079 
<br/><br/><label>Standard No.: </label>10.1136/bjo.2009.171892  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Base Sequence<br/>Chromosomes, Human, Pair 2--genetics<br/>Codon, Nonsense<br/>Electroretinography<br/>Female<br/>Genetic Linkage<br/>Genotype<br/>Humans<br/>Lod Score<br/>Male<br/>Middle Aged<br/>Pedigree<br/>Proto-Oncogene Proteins--genetics<br/>Receptor Protein-Tyrosine Kinases--genetics<br/>Retinitis Pigmentosa--genetics<br/>Visual Acuity<br/>c-Mer Tyrosine Kinase