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

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

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Publication Details

Journal
Journal of the American College of Cardiology
Published
2025-03-29
DOI
https://doi.org/10.1016/s0735-1097(25)01997-7
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
0.00
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article

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

Laura Robertson, John C. Stendahl, James S. Ware, Jeff Haroldson et al.
Journal of the American College of Cardiology
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

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

Laura Robertson, John C. Stendahl, James S. Ware, Jeff Haroldson, Dominic Abrams, William Harrison, Sara Saberi, Iacopo Olivotto, Joseph William Rossano, ANJALI TIKU OWENS, Rachel J. Lampert, Michelle Michels, Whedy Wang, Neal K. Lakdawala, Victoria Nicole Parikh, Kimberly Y. Lin, Carolyn Ho, Adam S. Helms, Sharlene M. Day, Thomas D. Ryan, Mark W. W. Russell, Bardha Varfaj, Whittemore G. Tingley, Euan A. Ashley, Jodie Ingles
article en

Abstract

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

Journal of the American College of CardiologyVol. 85(12)
Openalex Percentile: Top 91%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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