Identification of a novel exon3 deletion of RYR2 in a family with catecholaminergic polymorphic ventricular tachycardia-Reference-Cited by-同舟云学术

Identification of a novel exon3 deletion of RYR2 in a family with catecholaminergic polymorphic ventricular tachycardia

Author:

Dharmawan Tommy¹,Nakajima Tadashi¹^ORCID,Ohno Seiko²³,Iizuka Takashi¹,Tamura Shuntaro¹,Kaneko Yoshiaki¹,Horie Minoru³⁴,Kurabayashi Masahiko¹

Affiliation:

1. Department of Cardiovascular Medicine Gunma University Graduate School of Medicine Maebashi Japan

2. Department of Bioscience and Genetics National Cerebral and Cardiovascular Center Suita Japan

3. Department of Cardiovascular and Respiratory Medicine Shiga University of Medical Science Otsu Japan

4. Center for Epidemiologic Research in Asia Shiga University of Medical Science Otsu Japan

Funder

Japan Society for the Promotion of Science

Japan Agency for Medical Research and Development

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,General Medicine

Link

Reference32 articles.

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