A de novo ryanodine receptor 2 gene variant in a case of sudden cardiac death. [electronic resource]
Producer: 20201118Description: 619-623 p. digitalISSN:- 1437-1596
- Adult
- Autopsy
- Death, Sudden, Cardiac -- etiology
- High-Throughput Nucleotide Sequencing
- Humans
- Italy -- epidemiology
- Male
- Mutation, Missense
- Ryanodine Receptor Calcium Release Channel -- genetics
- Sequence Analysis, DNA
- Tachycardia, Ventricular -- genetics
- Polymorphic Catecholaminergic Ventricular Tachycardia
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Publication Type: Case Reports; Journal Article
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