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Nanomechanical phenotypes in cMyBP-C mutants that cause hypertrophic cardiomyopathy

Nanomechanical phenotypes in cMyBP-C mutants that cause hypertrophic cardiomyopathy

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2508165628

Nanomechanical phenotypes in cMyBP-C mutants that cause hypertrophic cardiomyopathy

About this item

Full title

Nanomechanical phenotypes in cMyBP-C mutants that cause hypertrophic cardiomyopathy

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

Journal title

bioRxiv, 2020-09

Language

English

Formats

Publication information

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

More information

Scope and Contents

Contents

ABSTRACT Hypertrophic cardiomyopathy (HCM) is a disease of the myocardium caused by mutations in sarcomeric proteins with mechanical roles, such as the molecular motor myosin. Around half of the HCM-causing genetic variants target contraction modulator cardiac myosin-binding protein C (cMyBP-C), although the underlying pathogenic mechanisms remain...

Alternative Titles

Full title

Nanomechanical phenotypes in cMyBP-C mutants that cause hypertrophic cardiomyopathy

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2508165628

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2508165628

Other Identifiers

E-ISSN

2692-8205

DOI

10.1101/2020.09.19.304618