Xu, Zhiwen
Lo, Wing-Sze
Beck, David B.
Schuch, Luise A.
Oláhová, Monika
Kopajtich, Robert
Chong, Yeeting E.
Alston, Charlotte L.
Seidl, Elias
Zhai, Liting
Lau, Ching-Fun
Timchak, Donna
LeDuc, Charles A.
Borczuk, Alain C.
Teich, Andrew F.
Juusola, Jane
Sofeso, Christina
Müller, Christoph
Pierre, Germaine
Hilliard, Tom
Turnpenny, Peter D.
Wagner, Matias
Kappler, Matthias
Brasch, Frank
Bouffard, John Paul
Nangle, Leslie A.
Yang, Xiang-Lei
Zhang, Mingjie
Taylor, Robert W.
Prokisch, Holger
Griese, Matthias
Chung, Wendy K.
Schimmel, Paul
Funding for this research was provided by:
aTyr Pharma
National Foundation for Cancer Research
Research Grants Council of Hong Kong (16100015)
JPB Foundation
Simons Foundation
NIH (R01GM088278)
chILD-EU (305653)
Bundesministerium für Bildung und Forschung
HCQ4Surfdefect
European Union (305663, A16125)
GENOMIT (01GM1603, 01GM1207)
EU Horizon2020 Collaborative Research Project SOUND (633974)
Else Kröner-Fresenius-Stiftung
European Cooperation in Science and Technology COST (A16125)
Wellcome Centre for Mitochondrial Research (203105/Z/16/Z)
Medical Research Council (MRC) Centre for Translational Research in Neuromuscular Disease
Mitochondrial Disease Patient Cohort (G0800674)
Lily Foundation
UK NHS Highly Specialized Service for Rare Mitochondrial Disorders of Adults and Children
This article is maintained by: Elsevier
Article Title: Bi-allelic Mutations in Phe-tRNA Synthetase Associated with a Multi-system Pulmonary Disease Support Non-translational Function
Journal Title: The American Journal of Human Genetics
CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.ajhg.2018.06.006
Content Type: article
Copyright: © 2018 The Authors.