PMC:4573257 / 27899-29058 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/4573257","sourcedb":"PMC","sourceid":"4573257","source_url":"https://www.ncbi.nlm.nih.gov/pmc/4573257","text":"Acknowledgments\nThis work was supported by grants from the Medical Research Council UK (MC_U105697135 to J.R., C.A.P., A.D., and M.M.), the German Bundesministerium für Bildung und Forschung through funding of the E-Rare project GENOMIT (01GM1207 to T.M. and H.P.), the German Network or Mitochondrial Disorders (01GM1113C and 01GM0866 to T.M., H.P., and M.S.), the Juniorverbund in der Systemmedizin “mitOmics” (FKZ 01ZX1405C to T.B.H.), the German Center for Heart Research (Z76010017300 and Z56010015300 to T.M.), the Wellcome Trust Strategic Award (096919/Z/11/Z to R.W.T. and P.F.C.), the Medical Research Council Centre for Neuromuscular Diseases (G0601943 to R.W.T. and P.F.C.), the UK National Health Service Highly Specialised “Rare Mitochondrial Disorders of Adults and Children” Service (C.L.A. and R.W.T.), the Lily Foundation (R.W.T.), a National Institute for Health Research doctoral fellowship (NIHR-HCS-D12-03-04 to C.L.A.), and Telethon Italy grant GGP11011 (C. Dallabona, C. Donnini, and I.F.). P.F.C. is a Wellcome Trust Senior Fellow in Clinical Science (101876/Z/13/Z) and a UK National Institute for Health Research Senior Investigator.","divisions":[{"label":"title","span":{"begin":0,"end":15}}],"tracks":[]}