MFSD7c functions as a transporter of choline at the blood–brain barrier
Mutations in the orphan transporter MFSD7c (also known as Flvcr2), are linked to Fowler
syndrome. Here, we used Mfsd7c knockout (Mfsd7c–/–) mice and cell-based assays to …
syndrome. Here, we used Mfsd7c knockout (Mfsd7c–/–) mice and cell-based assays to …
Integrative genetic analysis identifies FLVCR1 as a plasma-membrane choline transporter in mammals
Genome-wide association studies (GWASs) of serum metabolites have the potential to
uncover genes that influence human metabolism. Here, we combined an integrative genetic …
uncover genes that influence human metabolism. Here, we combined an integrative genetic …