'Rotor free-wheeling' in impaired F1FO-ATPase induces congenital hypermetabolism
Salvatore Nesci1, Giovanni Romeo2
1Department of Veterinary Medical Sciences, University of Bologna, 40064, Ozzano Emilia, Italy.
Abstract:
A de novo heterozygous variant in the catalytic subunit of mitochondrial F1FO-ATPase has been recently discovered by Ganetzky et al. to be the main cause of an autosomal dominant syndrome of hypermetabolism associated with defective ATP production. We describe how the 'rotor free-wheeling' causes this F1FO-ATPase dysfunction in primary congenital hypothyroidism.
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