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Article

Chronologic electrocardiographic changes in patients with hypertrophic cardiomyopathy associated with cardiac troponin 1 mutation.

American heart journal - 1 Feb 2002

Shimizu Masami, Ino Hidekazu, Yamaguchi Masato, Terai Hidenobu, Hayashi Kenshi, Kiyama Masaru, Sakata Kenji, Hayashi Tatsumi, Inoue Masaru, Kaneda Tomoya, Mabuchi Hiroshi

Abstract excerpt

BACKGROUND: Deletion of lysine 183 (K183del) in the cardiac troponin I (cTnI) gene is one of the mutations that causes hypertrophic cardiomyopathy (HCM). However, the phenotypic expression of this mutation has not been well established. METHODS AND RESULTS: We analyzed 10 probands with HCM associated with a K183del in the cTnI gene, as well as their family members. Forty-seven of these 80 subjects were found to...

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Identifiers

PMID: 11835033
DOI: 10.1067/mhj.2002.119760

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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