A Stargardt disease‐3 mutation in the mouse Elovl4 gene causes retinal deficiency of C32–C36 acyl phosphatidylcholines

Abstract
Stargardt disease‐3 (STGD3) is a juvenile dominant macular degeneration caused by mutations in elongase of very long chain fatty acid‐4. All identified mutations produce a truncated protein which lac...

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