Are substitutions in the first hypervariable region of the mitochondrial DNA displacement-loop in sudden infant death syndrome due to maternal inheritance?

Acta Paediatrica, International Journal of Paediatrics

Volumn 91, Issue 10, 2002, Pages 1060-1064

  Arnestad, M ^a   Opdal, S H ^a   Musse, M A ^a   Vege, A ^a   Rognum, T O ^a  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

Author keywords

D loop; HVR1; Inheritance; Mitochondrial DNA; SIDS

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; BASE PAIRING; CHROMOSOME SUBSTITUTION; CONTROLLED STUDY; DISEASE COURSE; ENVIRONMENTAL FACTOR; EXTRACHROMOSOMAL INHERITANCE; FEMALE; GENE MUTATION; GENE SEQUENCE; HAPLOTYPE; HUMAN; INFANT; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SUDDEN INFANT DEATH SYNDROME;

ADULT; COMPLEMENTARITY DETERMINING REGIONS; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; FEMALE; HUMANS; INFANT; INHERITANCE PATTERNS; SUDDEN INFANT DEATH;

EID: 0036399230     PISSN: 08035253     EISSN: None     Source Type: Journal    
DOI: 10.1080/080352502760311557     Document Type: Article

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