Mutations in the MYBPC3 gene are the leading genetic cause of Hypertrophic Cardiomyopathy (HCM) reducing levels of functional MYBP-c protein.

DIFFERENCES IN PATIENT CHARACTERISTICS AND BURDEN OF DISEASE IN ADULTS WITH MYBPC3-ASSOCIATED HCM / Wang, Whedy; Varfaj, Bardha; Robertson, Laura; Harrison, William; Haroldson, Jeff; Tingley, Whittemore; Lakdawala, Neal K.; Owens, Anjali Tiku; Saberi, Sara; Lin, Kimberly Y.; Stendahl, John; Parikh, Victoria; Ingles, Jodie; Ashley, Euan A.; Ware, James; Michels, Michelle; Lampert, Rachel J.; Abrams, Dominic J.; Rossano, Joseph William; Russell, Mark W.; Ryan, Thomas D.; Olivotto, Iacopo; Day, Sharlene M.; Ho, Carolyn; Helms, Adam. - In: JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY. - ISSN 0735-1097. - ELETTRONICO. - 85:(2025), pp. 0-0. [10.1016/s0735-1097(25)01997-7]

DIFFERENCES IN PATIENT CHARACTERISTICS AND BURDEN OF DISEASE IN ADULTS WITH MYBPC3-ASSOCIATED HCM

Olivotto, Iacopo
;
2025

Abstract

Mutations in the MYBPC3 gene are the leading genetic cause of Hypertrophic Cardiomyopathy (HCM) reducing levels of functional MYBP-c protein.
2025
85
0
0
Wang, Whedy; Varfaj, Bardha; Robertson, Laura; Harrison, William; Haroldson, Jeff; Tingley, Whittemore; Lakdawala, Neal K.; Owens, Anjali Tiku; Saberi...espandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1417464
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