Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome
- 31 July 1995
- journal article
- Published by Elsevier in Pediatric Neurology
- Vol. 13 (1), 69-72
- https://doi.org/10.1016/0887-8994(95)00082-q
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
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