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Kawabata K 1
Showing records 1 to 1 | Display all abstracts from Kawabata K13700 Clinical phenotype of a Japanese family with primary open-angle glaucoma caused by a Ala 363 Thr mutation in the MYOC gene
Ohyama A; Fujimaki T; Kimura T; Kawabata K; Fujiki K; Ishikawa K; Mashima Y; Murakami A
Nippon Ganka Gakkai Zasshi 2006; 110: 37-43
