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Homozygous and mutated SLC19A3 gene can cause various conditions such as biotin-thiamine responsive basal ganglia disease (BTBGD), lactic acidosis combined with encephalopathy, infantile epileptic spasms, and early childhood encephalopathy induced by disease or trauma

Zargari O, Kimyai-Asadi A, Jafroodi M

Patients with Crohns disease-an autoimmune disorder of digestive tract showed a reduction in Faecalibacterium and Roseburia spp

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Nov 10 2021 Ignatova et al., Russian Medical Inquiry, doi:10.32364/2587-6821-2021-5-7-473-478 Therapeutic possibilities of using an expectorant mucolytic agent with antioxidant properties in COVID-19 infection 20% shorter hospitalization (p=0.05)