Widespread tissue distribution of a tRNALeu(UUR) m... [Neurology. 1991] - PubMed

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Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene. [J Pediatr. 1992]
Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene.
Inui K, Fukushima H, Tsukamoto H, Taniike M, Midorikawa M, Tanaka J, Nishigaki T, Okada S. J Pediatr. 1992 Jan; 120(1):62-6.
A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). [Biochim Biophys Acta. 1991]
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Goto Y, Nonaka I, Horai S. Biochim Biophys Acta. 1991 Oct 21; 1097(3):238-40.
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Kobayashi Y, Momoi MY, Tominaga K, Momoi T, Nihei K, Yanagisawa M, Kagawa Y, Ohta S. Biochem Biophys Res Commun. 1990 Dec 31; 173(3):816-22.
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Cited by 10 PubMed Central articles

Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype. [Neurology. 2011]
Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype.
Kaufmann P, Engelstad K, Wei Y, Kulikova R, Oskoui M, Sproule DM, Battista V, Koenigsberger DY, Pascual JM, Shanske S, et al. Neurology. 2011 Nov 29; 77(22):1965-71. Epub 2011 Nov 16.
Longitudinal changes of mtDNA A3243G mutation load and level of functioning in MELAS. [Am J Med Genet A. 2009]
Longitudinal changes of mtDNA A3243G mutation load and level of functioning in MELAS.
Mehrazin M, Shanske S, Kaufmann P, Wei Y, Coku J, Engelstad K, Naini A, De Vivo DC, DiMauro S. Am J Med Genet A. 2009 Feb 15; 149A(4):584-7.
Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutation. [J Med Genet. 2007]
Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutation.
Pyle A, Taylor RW, Durham SE, Deschauer M, Schaefer AM, Samuels DC, Chinnery PF. J Med Genet. 2007 Jan; 44(1):69-74. Epub 2006 Sep 1.

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Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial D...
Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome.
Neurology. 1991 Oct ;41(10):1663-4.

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Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome.

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