Prostaglandins Other Lipid Mediat 142:4652 Alcalay RN, Mallet V, Vanderperre B, Tavassoly O, Dauvilliers Y, Wu RYJ, Ruskey JA, Leblond CS, Ambalavanan A, Laurent SB et al (2019) SMPD1 mutations, activity, and -synuclein accumulation in Parkinsons disease
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Mutations in the SLC19A3 gene are associated with thiamine metabolism dysfunction syndrome 2 (THMD2)
youre going to be able to talk about those findings