Matches in DBpedia 2016-04 for { ?s ?p "Hereditary folate malabsorption (HFM - OMIM #229050) is a rare autosomal recessive disorder caused by caused by loss-of-function mutations in the proton-coupled folate transporter (PCFT) gene, resulting in systemic folate deficiency and impaired delivery of folate to the brain."@en }
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- Hereditary_folate_malabsorption abstract "Hereditary folate malabsorption (HFM - OMIM #229050) is a rare autosomal recessive disorder caused by caused by loss-of-function mutations in the proton-coupled folate transporter (PCFT) gene, resulting in systemic folate deficiency and impaired delivery of folate to the brain.".
- Hereditary_folate_malabsorption comment "Hereditary folate malabsorption (HFM - OMIM #229050) is a rare autosomal recessive disorder caused by caused by loss-of-function mutations in the proton-coupled folate transporter (PCFT) gene, resulting in systemic folate deficiency and impaired delivery of folate to the brain.".