A novel RYR2 loss-of-function mutation (I4855M) is associated with left ventricular non-compaction and atypical catecholaminergic polymorphic ventricular tachycardia

詳細情報 詳細情報について

• CRID

  1363388845307109888

• DOI

  10.1016/j.jelectrocard.2016.09.006

• ISSN

  00220736

• Web Site

  https://api.elsevier.com/content/article/PII:S0022073616301790?httpAccept=text/plain

  https://api.elsevier.com/content/article/PII:S0022073616301790?httpAccept=text/xml

• データソース種別

  • Crossref