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Citation: Ke. Peltola et al., Ophthalmologic heterogeneity in subjects with gyrate atrophy of choroid and retina harboring the L402P mutation of ornithine aminotransferase, OPHTHALMOL, 108(4), 2001, pp. 721-729

Authors: Valtonen, M Nanto-Salonen, K Jaaskelainen, S Heinanen, K Alanen, A Heinonen, OJ Lundbom, N Erkintalo, M Simell, O

Citation: M. Valtonen et al., Central nervous system involvement in gyrate atrophy of the choroid and retina with hyperornithinaemia, J INH MET D, 22(8), 1999, pp. 855-866

Authors: Nanto-Salonen, K Komu, M Lundbom, N Heinanen, K Alanen, A Sipila, I Simell, O

Citation: K. Nanto-salonen et al., Reduced brain creatine in gyrate atrophy of the choroid and retina with hyperornithinemia, NEUROLOGY, 53(2), 1999, pp. 303-307

Authors: Heinanen, K Nanto-Salonen, K Komu, M Erkintalo, M Heinonen, OJ Pulkki, K Valtonen, M Nikoskelainen, E Alanen, A Simell, O

Citation: K. Heinanen et al., Muscle creatine phosphate in gyrate atrophy of the choroid and retina withhyperornithinaemia-clues to pathogenesis, EUR J CL IN, 29(5), 1999, pp. 426-431

Authors: Heinanen, K Nanto-Salonen, K Komu, M Erkintalo, M Alanen, A Heinonen, OJ Pulkki, K Nikoskelainen, E Sipila, I Simell, O

Citation: K. Heinanen et al., Creatine corrects muscle P-31 spectrum in gyrate atrophy with hyperornithinaemia, EUR J CL IN, 29(12), 1999, pp. 1060-1065