Associated Papers
Identification of a novel likely pathogenic TPM1 variant linked to hypertrophic cardiomyopathy in a family with sudden cardiac death.
Azimi A et al.
Esc Heart Failure, 2024
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
Walsh R et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017
27532257 (PubMed )
Supplement: gim201690x1.zip › Supplementary_Tables_resubmit.xlsx › Table_S1B
[Diseases in the field of internal medicine and gene abnormalities. 4. Molecular genetic analysis of hypertrophic cardiomyopathy among Japanese].
Kimura A
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine, 1996
[Case of Noonan syndrome with hypertrophic cardiomyopathy and a prominent outflow tract pressure gradient].
Kudo K et al.
Nihon Naika Gakkai Zasshi. the Journal of the Japanese Society of Internal Medicine, 1982
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