A missense mutation in the mitochondrial cytochrome β gene in a revisited case with histiocytoid cardiomyopathy

Pediatric Research

Volumn 48, Issue 3, 2000, Pages 311-314

  Andreu, Antoni L ^a,b   Checcarelli, Nicoletta ^a   Iwata, So ^c   Shanske, Sara ^a   Dimauro, Salvatore ^a  

^a Columbia College of Physicians and Surgeons ^*  (United States)

^b HOSPITAL UNIVERSITARI VALL D HEBRON   (Spain)

^c UPPSALA UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME B; MITOCHONDRIAL DNA; UBIQUINOL CYTOCHROME C REDUCTASE;

ARTICLE; CARDIOMYOPATHY; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; FEMALE; HISTIOCYTOID CARDIOMYOPATHY; HUMAN; INFANT; MISSENSE MUTATION; PRIORITY JOURNAL; PROTEIN STRUCTURE; SEQUENCE ANALYSIS; STRUCTURE ANALYSIS;

EID: 0033888963     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/00006450-200009000-00008     Document Type: Article

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