Millat, Gilles <br/><br/>
Functional characterization of putative novel splicing mutations in the cardiomyopathy-causing genes.  [electronic resource] 

 -  DNA and cell biology  Jul 2015 
 - 489-96 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1557-7430 
<br/><br/><label>Standard No.: </label>10.1089/dna.2015.2842  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alternative Splicing<br/>Animals<br/>Cardiomyopathy, Dilated--genetics<br/>Cardiomyopathy, Hypertrophic--genetics<br/>Carrier Proteins--genetics<br/>HeLa Cells<br/>Humans<br/>Point Mutation<br/>Polymorphism, Single Nucleotide<br/>RNA Splice Sites<br/>Rats<br/>Sequence Analysis, DNA<br/>Troponin T--genetics