Sabater-Molina, Marķa <br/><br/>
A Novel Founder Mutation in MYBPC3: Phenotypic Comparison With the Most Prevalent MYBPC3 Mutation in Spain.  [electronic resource] 

 -  Revista espanola de cardiologia (English ed.)  Feb 2017 
 - 105-114 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>1885-5857 
<br/><br/><label>Standard No.: </label>10.1016/j.rec.2016.06.020  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Aged<br/>Cardiomyopathy, Hypertrophic, Familial--epidemiology<br/>Carrier Proteins--genetics<br/>DNA--genetics<br/>DNA Mutational Analysis<br/>Echocardiography<br/>Female<br/>Founder Effect<br/>Genotype<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Myosins<br/>Pedigree<br/>Spain--epidemiology<br/>Survival Rate--trends