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A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)
scientific article (publication date: May 2004)
Author/s
author: Kári Stefánsson, Augustine Kong, Hreinn Stefansson, Jeffrey Gulcher, Ragnheidur Fossdal, Fridbert Jonasson
Work details
Publication date
May 1, 2004
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Language
English
Copyright status
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