A mitochondrial DNA microdeletion in a newborn girl with transient lactic acidosis
- 1 March 1996
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 19 (2) , 115-118
- https://doi.org/10.1007/bf01799407
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 genePediatric Neurology, 1995
- Uridine preserves the expression of respiratory enzyme deficiencies in cultured fibroblastsEuropean Journal of Pediatrics, 1993
- Sequence and organization of the human mitochondrial genomeNature, 1981
- Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.Proceedings of the National Academy of Sciences, 1977