Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders

Electrophoresis

Volumn 35, Issue 21-22, 2014, Pages 3111-3116

  Brion, Maria ^a,b   Blanco Verea, Alejandro ^a,b   Sobrino, Beatriz ^b,c   Santori, Montserrat ^a,c   Gil, Rocio ^a,b   Ramos Luis, Eva ^a,b   Martinez, Marina ^a,c   Amigo, Jorge ^b,c   Carracedo, Angel ^b,c,d  

^a Santiago University Clinical Hospital   (Spain)

^b Fundacion Publica Galega de Medicina Xenomica   (Spain)

^c UNIVERSITY OF SANTIAGO DE COMPOSTELA   (Spain)

^d KING ABDULAZIZ UNIVERSITY   (Saudi Arabia)

Author keywords

Arrhythmogenic disease; Genetic diagnosis; Next generation sequencing; Sudden cardiac death

Indexed keywords

GENES; HEART;

ARRHYTHMOGENIC DISEASE; CARDIAC DEATH; GENETIC DIAGNOSIS; GENETIC HETEROGENEITIES; HYBRIDISATION; NEXT-GENERATION SEQUENCING; PATHOGENICS; SUDDEN CARDIAC DEATH; SUDDEN DEATHS; YOUNG PEOPLES;

DIAGNOSIS;

DNA; POTASSIUM CHANNEL KCNQ1; SODIUM CHANNEL NAV1.5; GENETIC MARKER; PROTEIN;

ARRHYTHMOGENESIS; ARTICLE; CLINICAL ARTICLE; COMPUTER ANALYSIS; CONTROLLED STUDY; DNA HYBRIDIZATION; EXOME; FORENSIC MEDICINE; GENE; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; HEART ARRHYTHMIA; HUMAN; KCNH2 GENE; KCNQ1 GENE; NEXT GENERATION SEQUENCING; POLYMERASE CHAIN REACTION; SANGER SEQUENCING; SCN5A GENE; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; SUDDEN CARDIAC DEATH; VALIDATION PROCESS; DNA SEQUENCE; GENETIC MARKER; GENETICS; HIGH THROUGHPUT SEQUENCING; PROCEDURES;

ARRHYTHMIAS, CARDIAC; DEATH, SUDDEN, CARDIAC; GENETIC MARKERS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEINS; SEQUENCE ANALYSIS, DNA;

EID: 84917670380     PISSN: 01730835     EISSN: 15222683     Source Type: Journal    
DOI: 10.1002/elps.201400148     Document Type: Article

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