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Year | Number of Results |
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1989 | 1 |
1991 | 1 |
2002 | 1 |
2024 | 0 |
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An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.
Nature. 1989 May 25;339(6222):309-11. doi: 10.1038/339309a0.
Nature. 1989.
PMID: 2725645
Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies.
Servidei S, Zeviani M, Manfredi G, Ricci E, Silvestri G, Bertini E, Gellera C, Di Mauro S, Di Donato S, Tonali P.
Servidei S, et al.
Neurology. 1991 Jul;41(7):1053-9. doi: 10.1212/wnl.41.7.1053.
Neurology. 1991.
PMID: 2067633
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Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.
Lamantea E, Tiranti V, Bordoni A, Toscano A, Bono F, Servidei S, Papadimitriou A, Spelbrink H, Silvestri L, Casari G, Comi GP, Zeviani M.
Lamantea E, et al.
Ann Neurol. 2002 Aug;52(2):211-9. doi: 10.1002/ana.10278.
Ann Neurol. 2002.
PMID: 12210792
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