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Lemmela S 1
Showing records 1 to 1 | Display all abstracts from Lemmela S12261 Penetrance and phenotype of the Thr377Met Myocilin mutation in a large Finnish family with juvenile- and adult-onset primary open-angle glaucoma
Puska P; Lemmela S; Kristo P; Sankila EM; Jarvela I
Ophthalmic Genetics 2005; 26: 17-23