Open AccessLetter by Finsterer and Zarrouk-Mahjoub Regarding Article, “Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction”
Author(s) -
Josef Finsterer,
Sinda ZarroukMahjoub
Publication year - 2016
Publication title -
circulation cardiovascular genetics
Language(s) - English
Resource type - Journals
eISSN - 1942-325X
pISSN - 1942-3268
DOI - 10.1161/circgenetics.116.001630
Subject(s) - titin , missense mutation , cardiomyopathy , left ventricular noncompaction , mutation , genetics , medicine , cardiology , gene , biology , heart failure , sarcomere , myocyte
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