Mitochondrial DNA Mutations and Mitochondrial Abnormalities in Dilated Cardiomyopathy
Open Access
- 1 November 1998
- journal article
- Published by Elsevier in The American Journal of Pathology
- Vol. 153 (5) , 1501-1510
- https://doi.org/10.1016/s0002-9440(10)65738-0
Abstract
No abstract availableKeywords
This publication has 41 references indexed in Scilit:
- Mitochondrial disordersMolecular Human Reproduction, 1997
- Mitochondrial encephalomyopathies: what next?Journal of Inherited Metabolic Disease, 1996
- A Novel Mitochondrial DNA Point Mutation Associated with Mitochondrial EncephalocardiomyopathyBiochemical and Biophysical Research Communications, 1995
- A Novel mtDNA Point Mutation in Maternally Inherited CardiomyopathyBiochemical and Biophysical Research Communications, 1995
- A New Mitochondrial DNA Mutation Associated with Non-Insulin-Dependent Diabetes MellitusBiochemical and Biophysical Research Communications, 1995
- Accumulation of mtDNA with a Mutation at Position 3271 in tRNALeu(UUR) Gene Introduced from a Melas Patient to HeLa Cells Lacking mtDNA Results in Progressive Inhibition of Mitochondrial Respiratory FunctionBiochemical and Biophysical Research Communications, 1993
- Mitochondrial tRNAlle mutation in fatal cardiomyopathyBiochemical and Biophysical Research Communications, 1992
- PCR-SSCP: A method for detection of mutationsGenetic Analysis: Biomolecular Engineering, 1992
- Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathyBiochemical and Biophysical Research Communications, 1990
- Percutaneous Transvenous Endomyocardial Biopsy in Human Heart RecipientsThe Annals of Thoracic Surgery, 1973