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Dual myosin binding protein C3 and potassium voltage-gated channel subfamily H member 2 co-inherited pathogenic variants in a patient with hypertrophic cardiomyopathy and long QT 2 syndrome: A case report.

AuthorsChikezie K Alvarez, Emily Smith, Adaya Weissler-Snir
JournalHeartRhythm case reports (HeartRhythm Case Rep) Vol. 8 Issue 3 Pg. 200-204 (Mar 2022) ISSN: 2214-0271 [Print] United States
PMID35492841 (Publication Type: Case Reports)

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