Ophthalmologic heterogeneity in subjects with gyrate atrophy of choroid and retina harboring the L402P mutation of ornithine aminotransferase-Reference-Cited by-同舟云学术

Ophthalmologic heterogeneity in subjects with gyrate atrophy of choroid and retina harboring the L402P mutation of ornithine aminotransferase

Published:2001-04 Issue:4 Volume:108 Page:721-729
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Peltola Katja E,Näntö-Salonen Kirsti,Heinonen Olli J,Jääskeläinen Satu,Heinänen Kaarlo,Simell Olli,Nikoskelainen Eeva

Publisher

Elsevier BV

Subject

Ophthalmology

Reference25 articles.

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5. Reduced brain creatine in gyrate atrophy of the choroid and retina with hyperornithinemia;Näntö-Salonen;Neurology,1999

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