3.8 Article Data Paper

Pathogenic variant of RBM20 in a multiplex family with hypertrophic cardiomyopathy

Related references

Note: Only part of the references are listed.
Review Cardiac & Cardiovascular Systems

JCS/JHFS 2018 Guideline on the Diagnosis and Treatment of Cardiomyopathies

Hiroaki Kitaoka et al.

CIRCULATION JOURNAL (2021)

Article Cardiac & Cardiovascular Systems

Native T1 and Extracellular Volume in Transthyretin Amyloidosis

Ana Martinez-Naharro et al.

JACC-CARDIOVASCULAR IMAGING (2019)

Review Cardiac & Cardiovascular Systems

Myocardial T1 and ECV Measurement Underlying Concepts and Technical Considerations

Austin A. Robinson et al.

JACC-CARDIOVASCULAR IMAGING (2019)

Article Genetics & Heredity

Genetic background of Japanese patients with pediatric hypertrophic and restrictive cardiomyopathy

Takeharu Hayashi et al.

JOURNAL OF HUMAN GENETICS (2018)

Article Cardiac & Cardiovascular Systems

Hypertrophic Cardiomyopathy Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy

Ali J. Marian et al.

CIRCULATION RESEARCH (2017)

Article Cardiac & Cardiovascular Systems

Classification, Epidemiology, and Global Burden of Cardiomyopathies

William J. McKenna et al.

CIRCULATION RESEARCH (2017)

Article Cardiac & Cardiovascular Systems

Atlas of the clinical genetics of human dilated cardiomyopathy

Jan Haas et al.

EUROPEAN HEART JOURNAL (2015)

Article Cardiac & Cardiovascular Systems

Whole Exome Sequencing Identifies a Causal RBM20 Mutation in a Large Pedigree With Familial Dilated Cardiomyopathy

Quinn S. Wells et al.

CIRCULATION-CARDIOVASCULAR GENETICS (2013)

Article Cardiac & Cardiovascular Systems

Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy

Katharine M. Brauch et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2009)