A Stargardt disease‐3 mutation in the mouse Elovl4 gene causes retinal deficiency of C32–C36 acyl phosphatidylcholines
Open Access
- 5 November 2007
- journal article
- research article
- Published by Wiley in FEBS Letters
- Vol. 581 (28), 5459-5463
- https://doi.org/10.1016/j.febslet.2007.10.050
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...Keywords
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