Post-mortem analysis for two prevalent β-oxidation mutations in sudden infant death

Pediatrics International

Volumn 49, Issue 6, 2007, Pages 883-887

  Yang, Zi ^a   Lantz, Patrick E ^a   Ibdah, Jamal A ^a,b  

^a WAKE FOREST SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MISSOURI   (United States)

Author keywords

LCHAD; MCAD; Mitochondrial trifunctional protein; Sudden infant death (SID)

Indexed keywords

MEDIUM CHAIN ACYL COENZYME A DEHYDROGENASE; PARAFFIN;

ALPHA CHAIN; ARTICLE; CATALYST; CONTROLLED STUDY; DNA ISOLATION; FATTY ACID OXIDATION; FATTY LIVER; FEMALE; GENE MUTATION; HUMAN; HUMAN TISSUE; INFANT; LIVER HISTOLOGY; MAJOR CLINICAL STUDY; MALE; MEDICAL PRACTICE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SCREENING; SUDDEN INFANT DEATH SYNDROME; UNIVERSITY HOSPITAL;

ACYL-COA DEHYDROGENASE; AUTOPSY; FATTY LIVER; HUMANS; INFANT; LIVER; MULTIENZYME COMPLEXES; MUTATION; RETROSPECTIVE STUDIES; SUDDEN INFANT DEATH;

EID: 36648999598     PISSN: 13288067     EISSN: 1442200X     Source Type: Journal    
DOI: 10.1111/j.1442-200X.2007.02478.x     Document Type: Article

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