Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations
- 5 July 2002
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 295 (2), 342-347
- https://doi.org/10.1016/s0006-291x(02)00672-1
Abstract
No abstract availableKeywords
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