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This condition has been associated with maternal riboflavin deficiency, and supplementation with oral riboflavin led to the resolution of the clinical symptoms [70] A mitochondrial FAD transporter deficit has been reported in two cases of individuals who had mutations in both copies of the SLC25A32 gene (OMIM #616839), which encodes the mitochondrial FAD transporter
On the Ballestas Islands & Huacachina tour, youll see sea lions, penguins, pelicans, and the El Candelabro geoglyph from a boat
