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QuickView for FLVCR2;jsessionid=6BFB66A86286733EFAD82867E540E131;jsessionid=9C28F06DAF02F2C79A76E9FBBF8E541C;jsessionid=74F8BB5410D644287860372F2261439D;jsessionid=3C6553C8ACDE4B700E16FF85D4BC6F0A;jsessionid=FB27F4F4C179CA3C52FD6D01DFB2B1A0;jsessionid=22A764DE7514F01B04E1F45E01E58C2D;jsessionid=08E0AD1D62EB2D18BDC6689FEB40F305 (gene)
Most Relevant Literature
- MFSD7c functions as a transporter of choline at the blood-brain barrier.
- Structural and molecular basis of choline uptake into the brain by FLVCR2.
- Structural and molecular basis of choline uptake into the brain by FLVCR2.
- Deficiency of MFSD7c results in microcephaly-associated vasculopathy in Fowler syndrome.
- Cellular Functions and Molecular Mechanisms of the ESCRT Membrane-Scission Machinery.
Most Relevant Clinical Trials
There were no clinical trials for FLVCR2;jsessionid=6BFB66A86286733EFAD82867E540E131;jsessionid=9C28F06DAF02F2C79A76E9FBBF8E541C;jsessionid=74F8BB5410D644287860372F2261439D;jsessionid=3C6553C8ACDE4B700E16FF85D4BC6F0A;jsessionid=FB27F4F4C179CA3C52FD6D01DFB2B1A0;jsessionid=22A764DE7514F01B04E1F45E01E58C2D;jsessionid=08E0AD1D62EB2D18BDC6689FEB40F305
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