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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Ragnheidur Fossdal

deCODE Genetics

IS-101 Reykjavik



Name/email consistency: high



  • deCODE Genetics, IS-101 Reykjavik, Iceland. 2004


  1. A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration). Fossdal, R., Jonasson, F., Kristjansdottir, G.T., Kong, A., Stefansson, H., Gosh, S., Gulcher, J.R., Stefansson, K. Hum. Mol. Genet. (2004) [Pubmed]
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