Mitochondrial mutations in patients with congenital heart defects by next generation sequencing technology

Cardiology in the Young

Volumn 25, Issue 4, 2015, Pages 705-711

  Abaci, Neslihan ^a   Arikan, Muzaffer ^a   Tansel, Türkan ^b   Sahin, Nazli ^b   Cakiris, Aris ^a   Pacal, Ferda ^a   Sirma Ekmekci, Sema ^a   Gök, Emre ^b   Üstek, Duran ^a  

^a ISTANBUL UNIVERSITY   (Turkey)

^b ISTANBUL UNIVERSITY   (Turkey)

Author keywords

Congenital heart defects; mitochondrial mutations; next generation sequencing

Indexed keywords

MITOCHONDRIAL DNA; RIBOSOME RNA; TRANSFER RNA;

ARTICLE; CARDIOMYOPATHY; CLINICAL ARTICLE; CONGENITAL HEART DISEASE; DNA SEQUENCE; GENE AMPLIFICATION; GENE MUTATION; HEART SURGERY; HUMAN; HUMAN TISSUE; INFANT; MUTATIONAL ANALYSIS; NEWBORN; NEXT GENERATION SEQUENCING; POLYMERASE CHAIN REACTION; CARDIOMYOPATHIES; CONGENITAL HEART MALFORMATION; FEMALE; GENETICS; HIGH THROUGHPUT SEQUENCING; MALE; MUTATION; PRESCHOOL CHILD; PROCEDURES; TURKEY;

CARDIOMYOPATHIES; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; FEMALE; HEART DEFECTS, CONGENITAL; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; INFANT; INFANT, NEWBORN; MALE; MUTATION; POLYMERASE CHAIN REACTION; RNA, RIBOSOMAL; RNA, TRANSFER; SEQUENCE ANALYSIS, DNA; TURKEY;

EID: 84924479404     PISSN: 10479511     EISSN: 14671107     Source Type: Journal    
DOI: 10.1017/S1047951114000754     Document Type: Article

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