Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction

S Ohno, M Omura, M Kawamura, H Kimura, H Itoh… - Europace, 2014 - academic.oup.com
Aims Ryanodine receptor gene (RYR2) mutations are well known to cause
catecholaminergic polymorphic ventricular tachycardia (CPVT). Recently, RYR2 exon 3 …
被引用次数：105 相关文章
[PDF] archive.org

[PDF][PDF] Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction

S Ohno, M Omura, M Kawamura, H Kimura, H Itoh… - Europace, 2014 - scholar.archive.org
Aims Ryanodine receptor gene (RYR2) mutations are well known to cause
catecholaminergic polymorphic ventricular tachycardia (CPVT). Recently, RYR2exon 3 …

Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction.

S Ohno, M Omura, M Kawamura, H Kimura… - … : Journal of the …, 2014 - europepmc.org
AIMS: Ryanodine receptor gene (RYR2) mutations are well known to cause
catecholaminergic polymorphic ventricular tachycardia (CPVT). Recently, RYR2 exon 3 …

[引用][C] Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction

S Ohno, M Omura, M Kawamura, H Kimura, H Itoh… - Europace, 2014 - cir.nii.ac.jp

Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction

S Ohno, M Omura, M Kawamura… - … : journal of the …, 2014 - pubmed.ncbi.nlm.nih.gov
Aims Ryanodine receptor gene (RYR2) mutations are well known to cause
catecholaminergic polymorphic ventricular tachycardia (CPVT). Recently, RYR2 exon 3 …

[引用][C] Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction

S Ohno, M Omura, M Kawamura, H Kimura… - …, 2014 - Oxford University Press