Liver pathology in infantile mitochondrial DNA depletion syndrome

Pediatric and Developmental Pathology

Volumn 16, Issue 6, 2013, Pages 415-424

  Hazard, Florette K ^a   Ficicioglu, Can H ^b   Ganesh, Jaya ^b   Ruchelli, Eduardo D ^b  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

DNA depletion; Liver; Metabolic dysfunction; Mitochondria; Pediatric

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; AUTOPSY; CASE REPORT; CHOLESTASIS; CLINICAL FEATURE; CYTOPLASM; DISEASE COURSE; ELECTRON MICROSCOPY; FEMALE; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; HEMOSIDEROSIS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPEREOSINOPHILIA; INFANT; LACTIC ACIDOSIS; LIVER BIOPSY; LIVER CELL; LIVER DISEASE; LIVER FIBROSIS; LIVER MITOCHONDRION; LIVER STRUCTURE; METABOLIC DISORDER; MITOCHONDRIAL DNA DEPLETION SYNDROME; MUSCLE BIOPSY; MUTANT; PRIORITY JOURNAL; STEATOSIS;

EID: 84891767676     PISSN: 10935266     EISSN: 16155742     Source Type: Journal    
DOI: 10.2350/12-07-1229-OA.1     Document Type: Article

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