MtDNA-related idiopathic dilated cardiomyopathy [1]

European Journal of Human Genetics

Volumn 7, Issue 8, 1999, Pages 847-848

  Tessa, Alessandra ^a   Vilarinho, Laura ^b   Casali, Carlo ^c   Santorelli, Filippo M ^a  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^b NATIONAL INSTITUTE OF HEALTH DR RICARDO JORGE   (Portugal)

^c SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN; MITOCHONDRIAL DNA; NUCLEOTIDE; RIBOSOME RNA; TRANSFER RNA;

ANTICODON; CHILD; CHILDHOOD DISEASE; CLINICAL ARTICLE; CONGESTIVE CARDIOMYOPATHY; CONGESTIVE HEART FAILURE; CONTROLLED STUDY; FAMILY HISTORY; FEMALE; FIBROELASTOMA; GENE MUTATION; GENE SEQUENCE; HEART MUSCLE; HEART TRANSPLANTATION; HUMAN; LETTER; MALE; MITOCHONDRIAL RESPIRATION; MUSCLE BIOPSY; MUSCLE CONTRACTILITY; PRIORITY JOURNAL; PROTEIN SYNTHESIS; SIBLING;

EID: 0033378668     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200380     Document Type: Letter

References (5)

1. Dec GW, Fuster V: Idiopathic dilated cardiomyopathy. New Engl J Med 1994; 331: 1564-1575.
2. Michels VV, Moll PP, Miller FA et al: The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy. New Engl J Med 1992; 326: 77-82.
3. DiMauro S, Bonilla E: Mitochondrial encephalomyopathies. In: Rosenberg R, Prusiner S, DiMauro S, Barchi R (eds). The Molecular and Genetic Basis of Neurological Disease. Butterworth-Heinemann: Boston, 1997; 201-235.
4. Kogelnik AM, Lott MT, Brown MD, Navathe SB, Wallace DC: MITOMAP: a human mitochondrial genome database. Nucleic Acids Res 1996; 24: 177-179.
5. Antozzi C, Zeviani M: Cardiomyopathies in disorders of oxidative metabolism. Cardiovasc Res 1997; 35: 184-191.