Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease (Q70146023)

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scientific article published on 01 April 1991

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English	Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease	scientific article published on 01 April 1991

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9 October 2019

Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease (English)

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9 October 2019

Parkinson's disease

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9 October 2019

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T Ozawa

1

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9 October 2019

M Tanaka

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9 October 2019

H Ino

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9 October 2019

T Sano

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Y Wada

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9 October 2019

M Yoneda

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9 October 2019

Y Tanno

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9 October 2019

T Miyatake

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9 October 2019

T Tanaka

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1 April 1991

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9 October 2019

Biochemical and Biophysical Research Communications

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9 October 2019

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9 October 2019

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9 October 2019

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9 October 2019

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

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Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy

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Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

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Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy

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Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence

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Quantitative determination of deleted mitochondrial DNA relative to normal DNA in parkinsonian striatum by a kinetic PCR analysis

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Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature

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Mitochondrial leucine tRNA mutation in a mitochondrial encephalomyopathy

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Mitochondrial mutation in fatal infantile cardiomyopathy

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Direct sequencing of deleted mitochondrial DNA in myopathic patients

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Sequence and organization of the human mitochondrial genome

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Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome

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Sequence and gene organization of mouse mitochondrial DNA

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The complete nucleotide sequence of the Rattus norvegicus mitochondrial genome: cryptic signals revealed by comparative analysis between vertebrates

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Mitochondrial DNA polymorphism in Japanese. II. Analysis with restriction enzymes of four or five base pair recognition

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Mitochondrial DNA and human evolution

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Photolabelling of a mitochondrially encoded subunit of NADH dehydrogenase with [3H]dihydrorotenone.

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Mechanistic studies of ionizing radiation and oxidative mutagenesis: genetic effects of a single 8-hydroxyguanine (7-hydro-8-oxoguanine) residue inserted at a unique site in a viral genome.

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Disproportionate deficiency of iron-sulfur clusters and subunits of complex I in mitochondrial encephalomyopathy

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Sequence and expression of four mutant aspartic acid tRNA genes from the mitochondria of Saccharomyces cerevisiae

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Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

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Identifiers

10.1016/S0006-291X(05)80276-1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2025303%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2025303%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

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