Next-generation sequencing to identify genetic causes of cardiomyopathies

Current Opinion in Cardiology

Volumn 27, Issue 3, 2012, Pages 214-220

  Norton, Nadine ^a   Li, Duanxiang ^a   Hershberger, Ray E ^a  

^a UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

Author keywords

cardiomyopathy; exome; genetics; genomics; next generation sequencing

Indexed keywords

PROTEIN AARS2; PROTEIN ACSF3; PROTEIN BAG3; PROTEIN GATAD1; PROTEIN MRPL3; REGULATOR PROTEIN; UNCLASSIFIED DRUG;

BIOINFORMATICS; CARDIOMYOPATHY; CONGESTIVE CARDIOMYOPATHY; COPY NUMBER VARIATION; COST EFFECTIVENESS ANALYSIS; EPIGENETICS; EXOME; GENE DELETION; GENE INSERTION; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC TRAIT; GENETIC VARIABILITY; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; NEXT GENERATION SEQUENCE; PATHOGENICITY; PRIORITY JOURNAL; REVIEW; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; TRANSCRIPTOMICS;

CARDIOMYOPATHIES; COMPUTATIONAL BIOLOGY; EPIGENOMICS; EXOME; GENE DELETION; GENETIC VARIATION; HUMANS; MOLECULAR BIOLOGY; RISK ASSESSMENT; SEQUENCE ANALYSIS, DNA;

EID: 84862795516     PISSN: 02684705     EISSN: 15317080     Source Type: Journal    
DOI: 10.1097/HCO.0b013e328352207e     Document Type: Review

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