Mitochondrial DNA Mutations and Mitochondrial Abnormalities in Dilated Cardiomyopathy-Reference-Cited by-同舟云学术

Mitochondrial DNA Mutations and Mitochondrial Abnormalities in Dilated Cardiomyopathy

Published:1998-11 Issue:5 Volume:153 Page:1501-1510
ISSN:0002-9440
Container-title:The American Journal of Pathology
language:en
Short-container-title:The American Journal of Pathology

Author:

Arbustini Eloisa,Diegoli Marta,Fasani Roberta,Grasso Maurizia,Morbini Patrizia,Banchieri Nadia,Bellini Ornella,Dal Bello Barbara,Pilotto Andrea,Magrini Giulia,Campana Carlo,Fortina Paolo,Gavazzi Antonello,Narula Jagat,Viganò Mario

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference42 articles.

1. Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy;Ozawa;Biochem Biophys Res Commun,1990

2. Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNAGlycine gene;Merante;Am J Hum Genet,1994

3. Novel mtDNA point mutation in maternally inherited cardiomyopathy;Casali;Biochem Biophys Res Commun,1995

4. An additional mitochondrial tRNAIle point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy;Merante;Hum Mutat,1996

5. Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR);Zeviani;Lancet,1991

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