作者: Beth K. Potter , , Pranesh Chakraborty , Jonathan B. Kronick , Kumanan Wilson
DOI: 10.1038/GIM.2012.153
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摘要: This work was supported by a CIHR Emerging Team Grant (“Emerging team in rare diseases: acheiving the ‘triple aim’ for inborn errors of metabolism,” B.K. Potter, P. Chakraborty, and colleagues, 2012– 2017, grant no. TR3–119195). Current investigators collaborators in Canadian Inherited Metabolic Diseases Research Network are: J. Kronick, D. Coyle, K. Wilson, M. Brownell, R. Casey, A. Chan, S. Dyack, L. Dodds, Feigenbaum, D. Fell, M. Geraghty, C. Greenberg, Grosse, Guttmann, Khan, J. Little, B. Maranda, MacKenzie, Mhanni, F. Miller, G. Mitchell, J. Mitchell, Nakhla, Prasad, Siriwardena, K.N. Speechley, Stocker, Turner, H. Vallance, B.J. Wilson. Members of our external advisory board are Bidulka, T. Caulfield, J.T.R. Clarke, Doiron, El Emam, Evans, Kemper, W. McCormack, and Stephenson Julian. Little is Canada Research Chair Human Genome Epidemiology. Wilson a Canada Chair Public Health Policy.