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

Ophthalmology

Volumn 108, Issue 4, 2001, Pages 721-729

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

^a UNIVERSITY OF TURKU   (Finland)

^b TURKU UNIVERSITY HOSPITAL   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ORNITHINE OXOACID AMINOTRANSFERASE;

ADOLESCENT; ADULT; AMINO ACID METABOLISM; ARTICLE; CHILD; CHOROID GYRATE ATROPHY; CLINICAL ARTICLE; ELECTRORETINOGRAM; ENZYME ACTIVITY; ENZYME DEGRADATION; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC VARIABILITY; HUMAN; HYPERORNITHINEMIA; INFANT; MALE; PRIORITY JOURNAL; RETINA GYRATE ATROPHY; VISUAL FIELD; VISUAL IMPAIRMENT;

EID: 0035078026     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0161-6420(00)00587-X     Document Type: Article

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