FBXL4 is a mitochondria-localized protein in which autosomal recessive mutations cause multiple respiratory chain multisystem disease commonly involving cortical atrophy and leukodystrophy
Titel:
FBXL4 is a mitochondria-localized protein in which autosomal recessive mutations cause multiple respiratory chain multisystem disease commonly involving cortical atrophy and leukodystrophy
Auteur:
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 Polyak, Erzsebet Place, Emily Consugar, Mark Ostrovsky, Julian Vidoni, Sara Reyes, Aurelio Wong, Lee-Jun Sondheimer, Neal Salih, Mustafa Al-Jishi, Emtethal Freisinger, Peter Furlan, Francesca Lamperti, Costanza Rodenburg, Richard Pierce, Eric Smeitink, Jan Prokisch, Holger Alkuraya, Fowzan Zeviani, Massimo Falk, Marni J.