Mitochondrial mutation in fatal infantile cardiomyopathy
- 8 December 1990
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 336 (8728), 1452
- https://doi.org/10.1016/0140-6736(90)93162-i
Abstract
No abstract availableFunding Information
- Ministry of Health and Welfare
- Ministry of Education, Culture, Sports, Science and Technology (01-02-39)
This publication has 2 references indexed in Scilit:
- Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathyBiochemical and Biophysical Research Communications, 1990
- Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutationCell, 1990