Mitochondrial dysfunction in a novel form of autosomal recessive ataxia

Murad, Nor Azian Abdul, Cullen, Jason K, McKenzie, Matthew, Ryan, Michael T, Thorburn, David, Gueven, Nuri, Kobayashi, Junya, Birrell, Geoff, Yang, Jian, Dörk, Thilo, Becherel, Olivier, Grattan-Smith, Padraic and Lavin, Martin F 2013, Mitochondrial dysfunction in a novel form of autosomal recessive ataxia, Mitochondrion, vol. 13, no. 3, pp. 235-245, doi: 10.1016/j.mito.2012.11.006.

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Title Mitochondrial dysfunction in a novel form of autosomal recessive ataxia
Author(s) Murad, Nor Azian Abdul
Cullen, Jason K
McKenzie, MatthewORCID iD for McKenzie, Matthew
Ryan, Michael T
Thorburn, David
Gueven, Nuri
Kobayashi, Junya
Birrell, Geoff
Yang, Jian
Dörk, Thilo
Becherel, Olivier
Grattan-Smith, Padraic
Lavin, Martin F
Journal name Mitochondrion
Volume number 13
Issue number 3
Start page 235
End page 245
Total pages 11
Publisher Elsevier
Place of publication Amsterdam, The Netherlands
Publication date 2013-05
ISSN 1872-8278
Keyword(s) ataxia
DNA damage
amino acid substitution
chromosome disorders
cytochromes b
DNA mutational analysis
DNA, mitochondrial
electron transport
membrane potential, mitochondrial
mitochondrial diseases
mutation, missense
oxidative stress
protein stability
reactive oxygen species
tumor suppressor protein p53
science & technology
life sciences & biomedicine
cell biology
genetics & heredity
Language eng
DOI 10.1016/j.mito.2012.11.006
Field of Research 0604 Genetics
HERDC Research category C1.1 Refereed article in a scholarly journal
Copyright notice ©2012, Elsevier B.V.
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