The presence of multiple cellular defects associated with a novel G50E iron-sulfur cluster scaffold protein (ISCU) mutation leads to development of mitochondrial myopathy (Q39020569)

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scientific article published on 26 February 2014

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English	The presence of multiple cellular defects associated with a novel G50E iron-sulfur cluster scaffold protein (ISCU) mutation leads to development of mitochondrial myopathy	scientific article published on 26 February 2014

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scholarly article

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Europe PubMed Central

PMC publication ID

8 September 2017

The presence of multiple cellular defects associated with a novel G50E iron-sulfur cluster scaffold protein (ISCU) mutation leads to development of mitochondrial myopathy (English)

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

author name string

Prasenjit Prasad Saha

1

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Europe PubMed Central

PMC publication ID

8 September 2017

S K Praveen Kumar

2

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Europe PubMed Central

PMC publication ID

8 September 2017

Shubhi Srivastava

3

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Europe PubMed Central

PMC publication ID

8 September 2017

Devanjan Sinha

4

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PMC publication ID

8 September 2017

Gautam Pareek

5

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8 September 2017

Patrick D'Silva

6

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8 September 2017

language of work or name

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publication date

26 February 2014

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8 September 2017

Journal of Biological Chemistry

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8 September 2017

289

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Europe PubMed Central

PMC publication ID

8 September 2017

15

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Europe PubMed Central

PMC publication ID

8 September 2017

10359-10377

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Europe PubMed Central

PMC publication ID

8 September 2017

describes a project that uses

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4036159/fullTextXML

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The role of iron and reactive oxygen species in cell death

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1 reference

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based on heuristic

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Myopathy with lactic acidosis is linked to chromosome 12q23.3-24.11 and caused by an intron mutation in the ISCU gene resulting in a splicing defect

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Identifiers

10.1074/JBC.M113.526665

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

8 September 2017

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