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Kristjansdottir, Gudlaug Thora
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Kristjansdottir, Gudlaug Thora
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A novel TEAD1 mutation is the causative allele in Sveinsson's Chorioretinal Atrophy (helicoid peripapillary chorioretinal degeneration)
by
Fossdal, Ragnheidur
,
Jonasson, Fridbert
,
Kristjansdottir
,
Gudlaug
Thora
,
Kong, Augustine
,
Stefansson, Hreinn
,
Gosh, Shyamali
,
Gulcher, Jeffrey R.
,
Stefansson, Kari
Published in
Human Molecular Genetics
(2004)
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