Foti, Federica <br/><br/>
A de novo ryanodine receptor 2 gene variant in a case of sudden cardiac death.  [electronic resource] 

 -  International journal of legal medicine  Mar 2020 
 - 619-623 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1437-1596 
<br/><br/><label>Standard No.: </label>10.1007/s00414-019-02160-8  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Autopsy<br/>Death, Sudden, Cardiac--etiology<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Italy--epidemiology<br/>Male<br/>Mutation, Missense<br/>Ryanodine Receptor Calcium Release Channel--genetics<br/>Sequence Analysis, DNA<br/>Tachycardia, Ventricular--genetics<br/>Polymorphic Catecholaminergic Ventricular Tachycardia