Open AccessNGS data validated by Sanger sequencing reveal a puzzling small deletion of MYBPC3 gene associated with hypertrophic cardiomyopathy
Author(s) -
Miruna Mihaela Micheu,
NicoletaMonica PopaFotea,
NICOLETA OPRESCU,
Maria Dorobanțu,
Attila Cristian Rațiu,
Alexandru Al. Ecovoiu
Publication year - 2019
Publication title -
romanian biotechnological letters
Language(s) - English
Resource type - Journals
eISSN - 2248-3942
pISSN - 1224-5984
DOI - 10.25083/rbl/24.1/91.99
Subject(s) - hypertrophic cardiomyopathy , sanger sequencing , biology , genetics , mutation , gene , left ventricular noncompaction , breakpoint , dna sequencing , exon , computational biology , cardiomyopathy , medicine , cardiology , biochemistry , heart failure , chromosomal translocation
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