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Article

Identifying sarcomere gene mutations in hypertrophic cardiomyopathy: a personal history.

Circulation research - 18 Mar 2011

Seidman Christine E, Seidman J G

Abstract excerpt

This review provides an historical and personal perspective on the discovery of genetic causes for hypertrophic cardiomyopathy (HCM). Extraordinary insights by physicians who initially detailed remarkable and varied manifestations of the disorder, collaboration among multidisciplinary teams with skills in clinical diagnostics and molecular genetics, and hard work by scores of trainees solved the etiologic riddle...

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Share to Cardiomyopathy and Myosin Studies
Share to Cardiomyopathy, Hypertrophic
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 21415408
DOI: 10.1161/CIRCRESAHA.110.223834
PMCID: PMC3072749

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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