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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2000 | 1 |
2001 | 2 |
2003 | 1 |
2024 | 0 |
PubMed (cited) for id: 590100
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Novel homoplasmic mutation in the mitochondrial tRNATyr gene associated with atypical mitochondrial cytopathy presenting with focal segmental glomerulosclerosis.
Am J Med Genet A. 2003 Dec 1;123A(2):172-8. doi: 10.1002/ajmg.a.20315.
Am J Med Genet A. 2003.
PMID: 14598342
CPEO associated with a single nucleotide deletion in the mitochondrial tRNA(Tyr) gene.
Raffelsberger T, Rossmanith W, Thaller-Antlanger H, Bittner RE.
Raffelsberger T, et al.
Neurology. 2001 Dec 26;57(12):2298-301. doi: 10.1212/wnl.57.12.2298.
Neurology. 2001.
PMID: 11756614
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Functional characterisation of mitochondrial tRNA(Tyr) mutation (5877-->GA) associated with familial chronic progressive external ophthalmoplegia.
Sahashi K, Yoneda M, Ohno K, Tanaka M, Ibi T, Sahashi K.
Sahashi K, et al.
J Med Genet. 2001 Oct;38(10):703-5. doi: 10.1136/jmg.38.10.703.
J Med Genet. 2001.
PMID: 11594340
Free PMC article.
No abstract available.
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A novel mutation in the mitochondrial tRNA(TYr) gene associated with exercise intolerance.
Pulkes T, Siddiqui A, Morgan-Hughes JA, Hanna MG.
Pulkes T, et al.
Neurology. 2000 Oct 24;55(8):1210-2. doi: 10.1212/wnl.55.8.1210.
Neurology. 2000.
PMID: 11071502
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