FBXL4 is a mitochondria-localized protein in which autosomal recessive mutations cause multiple respiratory chain multisystem disease commonly involving cortical atrophy and leukodystrophy - Xiaowu Gai, Daniele Ghezzi, Mark A. Johnson, Caroline Biagosch, Hanah Shamseldin, Mai Tsukikawa, Claire Sheldon, Satish Srinivasan, Tobias Haack, Matteo Gorza, Thomas Wieland, Tim Strom, Erzsebet Polyak, Emily Place, Mark Consugar - Dissemin

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Elsevier, Mitochondrion, 6(13), p. 939-940

DOI: 10.1016/j.mito.2013.07.104

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FBXL4 is a mitochondria-localized protein in which autosomal recessive mutations cause multiple respiratory chain multisystem disease commonly involving cortical atrophy and leukodystrophy

Journal article published in 2013 by Xiaowu Gai, Daniele Ghezzi, Mark A. Johnson, Caroline Biagosch, Hanah Shamseldin, Mai Tsukikawa, Claire Sheldon, Satish Srinivasan, Tobias Haack, Matteo Gorza, Thomas Wieland, Tim Strom, Erzsebet Polyak, Emily Place, Mark Consugar and other authors.

This paper was not found in any repository, but could be made available legally by the author.

This paper was not found in any repository, but could be made available legally by the author.

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