Unusual presentation of propionic acidaemia as isolated cardiomyopathy

Journal of Inherited Metabolic Disease

Volumn 32, Issue SUPPL. 1, 2009, Pages

  Lee, T M ^a   Addonizio, L J ^a   Barshop, B A ^b   Chung, W K ^a,c  

^a Department of Medicine   (United States)

^b UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

^c Russ Berrie Medical Sciences Pavilion   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

METHYLMALONYL COENZYME A DECARBOXYLASE; PROPIONIC ACID; PROPIONIC ACID DERIVATIVE;

ADOLESCENT; ARTICLE; BLOOD; CARDIOMYOPATHY; CASE REPORT; ENZYMOLOGY; GENETICS; HEART TRANSPLANTATION; HUMAN; MALE; MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; PROPIONIC ACIDEMIA;

ADOLESCENT; BASE SEQUENCE; CARDIOMYOPATHIES; HEART TRANSPLANTATION; HUMANS; MALE; METHYLMALONYL-COA DECARBOXYLASE; MUTATION; PHENOTYPE; PROPIONATES; PROPIONIC ACIDEMIA;

EID: 84881017020     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-009-1084-1     Document Type: Article

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