Next generation sequence analysis for mitochondrial disorders

Genome Medicine

Volumn 1, Issue 10, 2009, Pages

  Vasta V , Valeria ^a   Ng B , Sarah ^b   Turner, Emily H ^b   Shendure, Jay ^b   Hahn, Si Houn ^a,c  

^a SEATTLE CHILDREN S RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

^c UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE; 3 HYDROXYACYL COENZYME A DEHYDROGENASE ALPHA SUBUNIT; MITOCHONDRIAL DNA; PYRUVATE DEHYDROGENASE; PYRUVATE DEHYDROGENASE ALPHA 1 SUBUNIT; UNCLASSIFIED DRUG;

ARTICLE; COST EFFECTIVENESS ANALYSIS; DISORDERS OF MITOCHONDRIAL FUNCTIONS; EXON; GENE MUTATION; GENE SEQUENCE; GENE TARGETING; GENETIC VARIABILITY; HETEROPLASMY; HETEROZYGOSITY; HUMAN; INTRON; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; RELIABILITY; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 76249100243     PISSN: None     EISSN: 1756994X     Source Type: Journal    
DOI: 10.1186/gm100     Document Type: Article

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