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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1980 | 1 |
1994 | 1 |
1997 | 1 |
2002 | 1 |
2003 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 8257
5 results
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Page 1
Decreased CCA-addition in human mitochondrial tRNAs bearing a pathogenic A4317G or A10044G mutation.
J Biol Chem. 2003 May 9;278(19):16828-33. doi: 10.1074/jbc.M213216200. Epub 2003 Mar 5.
J Biol Chem. 2003.
PMID: 12621050
Free article.
Exercise-induced muscle "burning," fatigue, and hyper-CKemia: mtDNA T10010C mutation in tRNA(Gly).
Nishigaki Y, Bonilla E, Shanske S, Gaskin DA, DiMauro S, Hirano M.
Nishigaki Y, et al.
Neurology. 2002 Apr 23;58(8):1282-5. doi: 10.1212/wnl.58.8.1282.
Neurology. 2002.
PMID: 11971101
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A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator.
Graham BH, Waymire KG, Cottrell B, Trounce IA, MacGregor GR, Wallace DC.
Graham BH, et al.
Nat Genet. 1997 Jul;16(3):226-34. doi: 10.1038/ng0797-226.
Nat Genet. 1997.
PMID: 9207786
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Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene.
Merante F, Tein I, Benson L, Robinson BH.
Merante F, et al.
Am J Hum Genet. 1994 Sep;55(3):437-46.
Am J Hum Genet. 1994.
PMID: 8079988
Free PMC article.
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Report of the WHO/ISFC task force on the definition and classification of cardiomyopathies.
[No authors listed]
[No authors listed]
Br Heart J. 1980 Dec;44(6):672-3. doi: 10.1136/hrt.44.6.672.
Br Heart J. 1980.
PMID: 7459150
Free PMC article.
No abstract available.
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