FBXL4 is a mitochondria-localized protein in which autosomal recessive mutations cause multiple respiratory chain multisystem disease commonly involving cortical atrophy and leukodystrophy
Gai, Xiaowu, Ghezzi, Daniele, Johnson, Mark A., Biagosch, Caroline, Shamseldin, Hanah, Tsukikawa, Mai, Sheldon, Claire, Srinivasan, Satish, Haack, Tobias, Gorza, Matteo, Wieland, Thomas, Strom, Tim, PVolume:
13
Language:
english
Journal:
Mitochondrion
DOI:
10.1016/j.mito.2013.07.104
Date:
November, 2013
File:
PDF, 72 KB
english, 2013