QuickView for FLVCR2;jsessionid=6BFB66A86286733EFAD82867E540E131;jsessionid=91FE0F732E44B9BC8B028F3CFE296733;jsessionid=552B5DBAFE52AD155990C4A257E2AA4A;jsessionid=57E5EF3201B718CF60C181A024400C1B;jsessionid=15B7FE836B35014D493716FB53A522C0;jsessionid=ED8E18E08D1071921C7A42A84C0ED7C0;jsessionid=9FAA96062FB23BCBA1A8D9A73F0A602C;jsessionid=C9FA875EBBCEAAB6C5596A45DD5A1ED2 (gene)

1. MFSD7c functions as a transporter of choline at the blood-brain barrier.
2. Structural and molecular basis of choline uptake into the brain by FLVCR2.
3. Structural and molecular basis of choline uptake into the brain by FLVCR2.
4. Deficiency of MFSD7c results in microcephaly-associated vasculopathy in Fowler syndrome.
5. Cellular Functions and Molecular Mechanisms of the ESCRT Membrane-Scission Machinery.

There were no clinical trials for FLVCR2;jsessionid=6BFB66A86286733EFAD82867E540E131;jsessionid=91FE0F732E44B9BC8B028F3CFE296733;jsessionid=552B5DBAFE52AD155990C4A257E2AA4A;jsessionid=57E5EF3201B718CF60C181A024400C1B;jsessionid=15B7FE836B35014D493716FB53A522C0;jsessionid=ED8E18E08D1071921C7A42A84C0ED7C0;jsessionid=9FAA96062FB23BCBA1A8D9A73F0A602C;jsessionid=C9FA875EBBCEAAB6C5596A45DD5A1ED2