Recent Mitochondrial DNA Mutations Increase the Risk of Developing Common Late-Onset Human Diseases

PLoS Genetics

Volumn 10, Issue 5, 2014, Pages

  Hudson, Gavin ^a   Gomez Duran, Aurora ^a   Wilson, Ian J ^a   Chinnery, Patrick F ^a  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ANKYLOSING SPONDYLITIS; ARTICLE; BRAIN ISCHEMIA; DISEASE ASSOCIATION; DISEASES; DNA SEQUENCE; GENE LOCUS; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HERITABILITY; HUMAN; HYPERTENSION; MITOCHONDRIAL GENOME; MULTIPLE SCLEROSIS; NON INSULIN DEPENDENT DIABETES MELLITUS; PARKINSON DISEASE; PHYLOGENY; PRIMARY BILIARY CIRRHOSIS; PROTEIN FUNCTION; PSORIASIS; RISK FACTOR; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; BILIARY CIRRHOSIS; GENETICS; MUTATION; OXIDATIVE PHOSPHORYLATION; ULCERATIVE COLITIS;

BRAIN ISCHEMIA; COLITIS, ULCERATIVE; DNA, MITOCHONDRIAL; HUMANS; LIVER CIRRHOSIS, BILIARY; MULTIPLE SCLEROSIS; MUTATION; OXIDATIVE PHOSPHORYLATION; PARKINSON DISEASE; PHYLOGENY; SCHIZOPHRENIA; SPONDYLITIS, ANKYLOSING;

EID: 84901614656     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1004369     Document Type: Article

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