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Biotin-thiamin-responsive basal ganglia disease Biotin-thiamin-responsive basal ganglia disease (also called biotin-responsive basal ganglia disease, thiamin transporter-2 deficiency, and thiamin metabolism dysfunction syndrome-2) is caused by an autosomal recessive mutation in the SLC19A3 gene that codes for THTR-2

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Ros pricing changes come amid intensifying competition in the subscription-based weight-loss treatment market, where platforms are racing to expand access to branded GLP-1 therapies while lowering upfront costs for patients