Impairment of tRNA processing by point mutations in mitochondrial tRNA(Leu)(UUR) associated with mitochondrial diseases (Q77323234)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9744809%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

title

Impairment of tRNA processing by point mutations in mitochondrial tRNA(Leu)(UUR) associated with mitochondrial diseases (English)

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4 December 2019

1

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4 December 2019

author name string

R M Karwan

series ordinal

2

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publication date

1 August 1998

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4 December 2019

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4 December 2019

volume

433

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4 December 2019

issue

3

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4 December 2019

page(s)

269-274

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4 December 2019

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Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

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Mitochondrial Encephalomyopathy Associated with a Novel Mutation in the Mitochondrial tRNAleu(UUR)Gene (A3243T)

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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A new point mutation at nucleotide pair 3291 of the mitochondrial tRNA(Leu(UUR)) gene in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)

7 January 2021

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7 January 2021

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7 January 2021

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10.1016/S0014-5793(98)00928-4

7 January 2021

Identifiers

DOI

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4 December 2019

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