(Q71523757)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8803815%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

title

The T-C(8356) mitochondrial DNA mutation in a Japanese family (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8803815%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

author name string

M Sano

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8803815%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

M Ozawa

2

1 reference

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19 October 2019

S Shiota

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8803815%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

Y Momose

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8803815%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

M Uchigata

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8803815%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

Y Goto

6

1 reference

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19 October 2019

publication date

1 June 1996

1 reference

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19 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8803815%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

volume

243

1 reference

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19 October 2019

issue

6

1 reference

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19 October 2019

page(s)

441-444

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00900496

19 October 2019

exact match

0 references

cites work

Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes

1 reference

12 December 2020

A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene

1 reference

12 December 2020

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

1 reference

12 December 2020

A common mitochondrial DNA mutation in the t-RNA(Lys) of patients with myoclonus epilepsy associated with ragged-red fibers

1 reference

12 December 2020

Variability in the activity of respiratory chain enzymes in mitochondrial myopathies

1 reference

12 December 2020

Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF).

1 reference

12 December 2020

Myoclonic epilepsy and ragged-red fibers with cytochrome oxidase deficiency: neuropathology, biochemistry, and molecular genetics

1 reference

12 December 2020

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

1 reference

12 December 2020

Maternally inherited mitochondrial myopathy and myoclonic epilepsy.

1 reference

12 December 2020

MELAS: clinical features, biochemistry, and molecular genetics

1 reference

12 December 2020

A new mtDNA mutation in the tRNA(Lys) gene associated with myoclonic epilepsy and ragged-red fibers (MERRF)

1 reference

12 December 2020

Mitochondrial myopathies

1 reference

12 December 2020

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation

1 reference

12 December 2020

Cerebral metabolism of oxygen and glucose in a patient with MELAS syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00900496

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8803815%20AND%20SRC:MED&resulttype=core&format=json

19 October 2019

1 reference