Work

MOESM1 of Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome

Year: 2017
Type: article
Abstract: Additional file 1: Table S1. List of genes sequenced for the proband.
Source: Figshare
Language: English
Field: Medicine
Open Access status: green
OpenAlex ID: W7136048780
FWCI:
Cites:
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Related to: 10