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Int J Mol Sci (2016) 17:116
HMN type VII is distinguished by vocal cord paresis and may be due to dominant mutations in SLC5A7 ( CHT ) [41], or DCTN1 [42]
L.HamiltonJ.TabriziS
Triiodothyronine-induced accumulations of malic enzyme, fatty acid synthase, acetyl-coenzyme A carboxylase, and their mRNAs are blocked by protein kinase inhibitors
