Differences in Patient Characteristics and Burden of Disease in Adults With Mybpc3-associated Hcm
Year: 2025
Type: article
Abstract: Mutations in the MYBPC3 gene are the leading genetic cause of Hypertrophic Cardiomyopathy (HCM) reducing levels of functional MYBP-c protein.
Authors: Whedy Wang, Bardha Varfaj, Laura Robertson, William Harrison, Jeff Haroldson, Whittemore Tingley, Neal K. Lakdawala, Anjali Tiku Owens, Sara Saberi, Kimberly Y. Lin, John Stendahl, Victoria Parikh, Jodie Ingles, Euan A. Ashley, James Ware, Michelle Michels, Rachel J. Lampert, Dominic J. Abrams, Joseph William Rossano, Mark W. Russell, Thomas D. Ryan, Iacopo Olivotto, Sharlene M. Day, Carolyn Ho, Adam Helms
Language: English
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $7,166
OpenAlex ID: W4408962579