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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   Peer reviewed

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, …
Mitochondrion, Vol.13(6), pp.939-940
11/2013
DOI: https://doi.org/10.1016/j.mito.2013.07.104

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