SLC19A1geneVitamin B12Autism spectrum disorders (ASD) are characterized by clinical heterogeneity and may be associated with cerebral folate deficiency (CFD). Among the causes, folate receptor alpha autoantibodies (FRAA) and variants of theSLC19A1gene are commonly highlighted. The aim of this study...
Single Nucleotide Polymorphisms of MTHFR (rs1051266) and SLC19A1 (rs1801133) Associated to Genomic Ancestry in Cuban Healthy PopulationSingle nucleotide polymorphismmethotrexatemethylenetetrahydrofolate reductasesolute carrier family 19 member 1ancestry