Articles with public access mandates - Michael Snyder - Austrian Science FundLearn more
OverallNIHNSFHHMIAHAWellcomeSNSFEuropean CommissionMTADOENIHRVACIHRDFGMRCGatesNSERCNSFCGovernment of SpainDoDNKFIKnut and Alice Wallenberg FoundationSwedish Research CouncilDamon Runyon Cancer Research FoundationCZIState of CalifoniaNHMRCMotor Neurone Disease Association, UKGenome CanadaDFFBBSRCBHFCancer Research UKDoris Duke Charitable FoundationLeducq Foundation, USASusan G. KomenNASAFWODNRFOTKAFormasDHFGovernment of ItalyVillum FoundationINSERMBMBFCPRITGBMFFRQSCASEMBLAcademy of FinlandNWOAcademy of Medical Sciences, UKZonMwANRKWFTUBITAKRWJFUSDAFWFARCHSFDBTTelethonESRCNational Centre for the Replacement, Refinement and Reduction of Animals in Research, UKWHOFondazione CariploKNAWNMRCUK Research & InnovationCGIARV Foundation, USALung Cancer Research Foundation, USABrain Tumour Charity, UKCarlsberg Foundation DKHFSP
Available based on mandate: 1
Biallelic mutations in ATP5F1D, which encodes a subunit of ATP synthase, cause a metabolic disorder
M Oláhová, WH Yoon, K Thompson, S Jangam, L Fernandez, ...
The American Journal of Human Genetics 102 (3), 494-504, 2018
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