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Open access

Case report

First published 2021-4

Heterozygous desmin gene ( DES ) mutation contributes to familial dilated cardiomyopathy

Ying-shuo Huang, Yun-li Xing, Hong-wei Li

Journal of International Medical Research

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Other

First published 2007-07

Novel Mutation in Splicing Donor of Dystrophin Gene First Exon in a Patient With Dilated Cardiomyopathy but No Clinical Signs of Skeletal Myopathy

Shigemi Kimura, Makoto Ikezawa, Shiro Ozasa [...]

Journal of Child Neurology

Free access

Research article

First published 2010-6

Mutations in the β-Myosin Heavy Chain Gene in Southern Chinese Families with Hypertrophic Cardiomyopathy

DD Zheng, JH Yang, Q Tao [...]

Journal of International Medical Research

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Research article

First published 2023-5

A novel deletion mutation accompanied by a point mutation in Lamin A/C gene: Screened from a dilated cardiomyopathy family

Hao Jia, Yongxin Sun, Wangchao Yao [...]

Perfusion

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Research article

First published 1997-4

Prognostic Significance of β-Myosin Heavy Chain Mutations is Reflective of Their Hypertrophic Expressivity in Patients with Hypertrophic Cardiomyopathy

Antoine Abchee, Ali J. Marian

Journal of Investigative Medicine

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Other

First published 2001-07

A5814G Mutation in Mitochondrial DNA Can Cause Mitochondrial Myopathy and Cardiomyopathy

Charalampos Karadimas, Kurenai Tanji, Maciej Geremek [...]

Journal of Child Neurology

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Research article

First published 2015-8

X-linked Recessive Distal Myopathy With Hypertrophic Cardiomyopathy Caused by a Novel Mutation in the FHL1 Gene

Colleen D’Arcy, Voula Kanellakis, Robin Forbes [...]

Journal of Child Neurology

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Research article

First published 2016-11

Spectrum of Mutations in Hypertrophic Cardiomyopathy Genes Among Tunisian Patients

Nawel Jaafar, Juan Gómez, Ikram Kammoun [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2012-06

Identification of Novel Mutations in LMNA Associated with Familial Forms of Dilated Cardiomyopathy

Birgit Stallmeyer, Matthias Koopmann, Eric Schulze-Bahr

Genetic Testing and Molecular Biomarkers

Retricted access

Case report

First published 2015-3

The Importance of Genetic Testing in a Case of Sudden Death in Hypertrophic Cardiomyopathy due to Troponin I Mutation

Vivian S. Snyder, Rick Bains, Philip S. Fitchev [...]

Academic Forensic Pathology

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