Varaico: Literature-Extracted Genetic Variants

Gene:PRRT2
Variant:p.K178E
Back to variants list

PRRT2

NM_145239.3:p.K178E

Associated Papers

Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?

Willott RH et al.

Journal of Molecular and Cellular Cardiology, 2010

Inherited cardiomyopathies as a troponin disease.

Harada K et al.

The Japanese Journal of Physiology, 2004

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."