Work

Abstract 4363582: A Rare Case of Genetic Cardiomyopathy: SCN5A mutation-associated Multifocal Ectopic Premature Purkinje-related Complexes Syndrome with Heart Failure with Improved Ejection Fraction

Year: 2025
Type: conference-abstract
Source: Circulation
Language: English
Field: Medicine
Open Access status: closed
OpenAlex ID: W4415790371
Cites:
Cited by:
Related to: