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.; Carolyn, Ho; Helms, Adam

doi:10.1016/s0735-1097(25)01997-7

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, W., Varfaj, B., Robertson, L., Harrison, W., Haroldson, J., Tingley, W., Lakdawala, N.K., Owens, A.T., Saberi, S., Lin, K.Y., Stendahl, J., Parikh, V., Ingles, J., Ashley, E.A., Ware, J., Michels, M., Lampert, R.J., Abrams, D.J., Rossano, J.W., Russell, M.W., et al.. - In: JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY. - ISSN 0735-1097. - ELETTRONICO. - 85:(2025), pp. 0-0. [10.1016/s0735-1097(25)01997-7]