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Article

A novel homozygous premature stop mutation in TNNT2 associates with Feline cardiomyopathy

2020-01-23

Abstract excerpt

<title>Abstract</title> <p>Background: Hypertrophic cardiomyopathy (HCM) is a genetic disease of the heart and the most common cause of sudden cardiac death in the young. HCM is considered a disease of the sarcomere owing to the large number of mutations in genes encoding sarcomeric proteins. The riddle lies in discovering how these mutations lead to disease. As a result, treatments to prevent and/or treat HCM ar...

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Literature Corpus work
5f28284a-7deb-5d7c-8896-cd532797e1ca
DOI
10.21203/rs.2.21647/v1
Open publication

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A novel homozygous premature stop mutation in TNNT2 associates with Feline cardiomyopathyDOI 10.21203/rs.2.21647/v1
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