Ragnheidur Fossdal
deCODE Genetics
IS-101 Reykjavik
Iceland
Name/email consistency: high
- 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)