I. Sipila

Mice lacking ornithine–δ–amino–transferase have paradoxical neonatal hypoornithinaemia and retinal degeneration

D. Valle, A. Milam, G. Steel, 1995, Nature Genetics.

Consensus statement - Prader-Willi syndrome: Growth hormone (GH)/insulin-like growth factor axis deficiency and GH treatment

D. Wilson, M. Cappa, G. Chiumello, 2000 .

At least two mutant alleles of ornithine 6-aminotransferase cause gyrate atrophy of the choroid and retina in Finns (RNase A protection/polymerase chain reaction/hyperornithinemia/chorioretinal degeneration/missense mutation)

C. Obie, D. Valle, M. Kaiser-Kupfer, 2016 .

Mice lacking ornithine-delta-aminotransferase have paradoxical neonatal hypoornithinaemia and retinal degeneration.

D. Valle, A. Milam, G. Steel, 1995, Nature genetics.

Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences.

C. Obie, D. Valle, M. Kaiser-Kupfer, 1992, The Journal of biological chemistry.

At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.

C. Obie, M. Kaiser-Kupfer, G. Mitchell, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Differences in linear growth and cortisol production between liver and renal transplant recipients on similar immunosuppression.

R. Koistinen, I. Sipila, C. Holmberg, 1995, Transplantation.

CHARACTERIZATION OF MUTANT LIVER

I. Sipila, 2022 .