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Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases.
FASEB J. 1992 Jul;6(10):2791-9. doi: 10.1096/fasebj.6.10.1634041.
FASEB J. 1992.
PMID: 1634041
Review.
Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.
Brown MD, Voljavec AS, Lott MT, Torroni A, Yang CC, Wallace DC.
Brown MD, et al.
Genetics. 1992 Jan;130(1):163-73. doi: 10.1093/genetics/130.1.163.
Genetics. 1992.
PMID: 1732158
Free PMC article.
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Mitochondrial tRNA(Thr) mutations and lethal infantile mitochondrial myopathy.
Brown MD, Torroni A, Shoffner JM, Wallace DC.
Brown MD, et al.
Am J Hum Genet. 1992 Aug;51(2):446-7.
Am J Hum Genet. 1992.
PMID: 1379415
Free PMC article.
No abstract available.
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A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.
Brown MD, Yang CC, Trounce I, Torroni A, Lott MT, Wallace DC.
Brown MD, et al.
Am J Hum Genet. 1992 Aug;51(2):378-85.
Am J Hum Genet. 1992.
PMID: 1322638
Free PMC article.
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