Altmann, Helene M <br/><br/>
Homozygous/Compound Heterozygous Triadin Mutations Associated With Autosomal-Recessive Long-QT Syndrome and Pediatric Sudden Cardiac Arrest: Elucidation of the Triadin Knockout Syndrome.  [electronic resource] 

 -  Circulation  Jun 2015 
 - 2051-60 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1524-4539 
<br/><br/><label>Standard No.: </label>10.1161/CIRCULATIONAHA.115.015397  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Carrier Proteins--genetics<br/>Child<br/>Child, Preschool<br/>Defibrillators, Implantable<br/>Exome<br/>Female<br/>Frameshift Mutation<br/>Genes, Recessive<br/>Heart Arrest--diagnosis<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Infant<br/>Long QT Syndrome--diagnosis<br/>Male<br/>Middle Aged<br/>Muscle Proteins--genetics<br/>Pedigree<br/>Phenotype<br/>Sequence Analysis, DNA<br/>Sympathectomy<br/>Syncope--diagnosis<br/>Syndrome<br/>Treatment Outcome<br/>Young Adult