Cardiomyopathy and kidney disease in a patient with maternally inherited diabetes and deafness caused by the 3243A>G mutation of mitochondrial DNA

Cardiology

Volumn 115, Issue 1, 2009, Pages 71-74

  Azevedo, Olga ^a   Vilarinho, Laura ^b   Almeida, Filipa ^a   Ferreira, Francisco ^a   Guardado, Joana ^a   Ferreira, Mariana ^b   Lourenço, António ^a   Medeiros, Rosa ^a   Almeida, João ^a  

^a Centro Hospitalar Do Alto Ave   (Portugal)

^b NATIONAL INSTITUTE OF HEALTH   (Portugal)

Author keywords

Cardiomyopathy; Heart failure; Left ventricular hypertrophy

Indexed keywords

ADENINE; CARNITINE; GUANINE; MITOCHONDRIAL DNA; TRANSFER RNA; UBIDECARENONE;

ADULT; ARTICLE; CARDIOMYOPATHY; CASE REPORT; CLINICAL FEATURE; DIABETES MELLITUS; DISEASE COURSE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; EXTRACHROMOSOMAL INHERITANCE; FAMILY HISTORY; HUMAN; KIDNEY DISEASE; MALE; NUCLEOTIDE SEQUENCE; PERCEPTION DEAFNESS; PHENOTYPIC VARIATION; PRIORITY JOURNAL; RNA GENE; SYMPTOM;

CARDIOMYOPATHIES; DEAFNESS; DIABETES MELLITUS; DNA, MITOCHONDRIAL; HUMANS; MALE; MIDDLE AGED; MITOCHONDRIAL DISEASES; POINT MUTATION;

EID: 70350425652     PISSN: 00086312     EISSN: None     Source Type: Journal    
DOI: 10.1159/000252811     Document Type: Article

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