Martin, Marcel <br/><br/>
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3.  [electronic resource] 

 -  Nature genetics  Aug 2013 
 - 933-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1546-1718 
<br/><br/><label>Standard No.: </label>10.1038/ng.2674  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Aneuploidy<br/>Chromosomes, Human, Pair 3<br/>DNA Copy Number Variations<br/>Eukaryotic Initiation Factor-1--chemistry<br/>Exome<br/>Female<br/>Gene Expression Profiling<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Male<br/>Melanoma--genetics<br/>Microsatellite Repeats<br/>Molecular Sequence Data<br/>Monosomy--genetics<br/>Mutation<br/>Neoplasm Metastasis<br/>Phosphoproteins--genetics<br/>Prognosis<br/>RNA Splicing Factors<br/>Ribonucleoprotein, U2 Small Nuclear--genetics<br/>Sequence Alignment<br/>Uveal Neoplasms--genetics<br/>Uveal Melanoma