1 resultado para Homozygous mutation
em Aberdeen University
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Mutation of SLC35D3 causes metabolic syndrome by impairing dopamine signaling in striatal D1 neurons
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Funding: This work was partially supported by grants from National Basic Research Program of China (2013CB530605; 2014CB942803), from National Natural Science Foundation of China 1230046; 31071252; 81101182) and from Chinese Academy of Sciences (KSCX2-EW-R-05, KJZD-EW-L08). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.