(Q43814295)

27 November 2017

title

A novel nonsense mutation (Q352X) in the mitochondrial cytochrome b gene associated with a combined deficiency of complexes I and III. (English)

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27 November 2017

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27 November 2017

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27 November 2017

Massimo Zeviani

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27 November 2017

Franco Carrara

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27 November 2017

Caterina Mariotti

series ordinal

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27 November 2017

Lucia Morandi

series ordinal

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27 November 2017

publication date

1 January 2002

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27 November 2017

published in

Neuromuscular Disorders

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27 November 2017

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27 November 2017

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27 November 2017

page(s)

49-52

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27 November 2017

cites work

Mitochondrial Disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900244-9

7 January 2021

A novel gly290asp mitochondrial cytochrome b mutation linked to a complex III deficiency in progressive exercise intolerance

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900244-9

7 January 2021

Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900244-9

7 January 2021

A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900244-9

7 January 2021

Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900244-9

7 January 2021

A missense mutation in the mitochondrial cytochrome b gene in a revisited case with histiocytoid cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900244-9

7 January 2021

A novel mutation (8342G→A) in the mitochondrial tRNALys gene associated with progressive external ophthalmoplegia and myoclonus

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900244-9

7 January 2021

Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2801%2900244-9

7 January 2021

10.1016/S0960-8966(01)00244-9

Identifiers

DOI

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27 November 2017

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