A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)
- 31 December 1990
- journal article
- case report
- Published by Elsevier BV in Biochemical and Biophysical Research Communications
- Vol. 173 (3), 816-822
- https://doi.org/10.1016/s0006-291x(05)80860-5
Abstract
No abstract availableKeywords
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