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1992 | 1 |
1996 | 1 |
2024 | 0 |
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Isolated case of mental retardation and ataxia due to a de novo mitochondrial T8993G mutation.
Am J Hum Genet. 1996 Mar;58(3):636-8.
Am J Hum Genet. 1996.
PMID: 8644724
Free PMC article.
No abstract available.
Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy.
Yoneda M, Chomyn A, Martinuzzi A, Hurko O, Attardi G.
Yoneda M, et al.
Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11164-8. doi: 10.1073/pnas.89.23.11164.
Proc Natl Acad Sci U S A. 1992.
PMID: 1454794
Free PMC article.
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