The embryological basis of subclinical hypertrophic cardiomyopathy

The embryological basis of subclinical hypertrophic cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is caused by mutations in sarcomeric proteins, the commonest being MYBPC3 encoding myosin-binding protein C. It is characterised by left ventricular hypertrophy but there is an important pre-hypertrophic phenotype with features including crypts, abnormal mitral leaf...

Full description

Bibliographic Details
Main Authors: Captur, Gabriella, Ho, Carolyn Y., Schlossarek, Saskia, Kerwin, Janet, Mirabel, Mariana, Wilson, Robert, Rosmini, Stefania, Obianyo, Chinwe, Reant, Patricia, Bassett, Paul, Cook, Andrew C., Lindsay, Susan, McKenna, William J., Mills, Kevin, Elliott, Perry M., Mohun, Timothy J., Carrier, Lucie, Moon, James C.
Format: Online
Language:English
Published: Nature Publishing Group 2016
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914973/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914973/

Similar Items