Granular corneal dystrophy with homozygous mutations in the kerato- epithelin gene [3] (multiple letters)

American Journal of Ophthalmology

Volumn 129, Issue 3, 2000, Pages 411-412

  Moller, H U ^a   Ridgway, A E A ^a   Okada, Masaki ^a   Yamamoto, Shuji ^a   Watanabe, Hitoshi ^a   Shimomura, Yoshikazu ^a   Tano, Yasuo ^a  

^a NONE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CORNEA DYSTROPHY; GENE MUTATION; GENETIC RISK; HUMAN; JAPAN; LETTER; PRIORITY JOURNAL;

CORNEAL DYSTROPHIES, HEREDITARY; EXTRACELLULAR MATRIX PROTEINS; HUMANS; MUTATION; NEOPLASM PROTEINS; TRANSFORMING GROWTH FACTOR BETA;

EID: 0033995242     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(00)00347-0     Document Type: Letter

References (4)

1. H.U. Moller A.E.A. Ridgway Granular corneal dystrophy Groenouw type I a report of a probable homozygous patient Acta Ophthalmol (Copenh) 68 1990 97 101
2. Moller HU. Granular corneal dystrophy Groenouw type I: clinical and genetic aspects. Acta Ophthalmol (Copenh) 1991;69 (suppl 198): Ph.D. Theses.
3. H.U. Moller Inter-familial variability and intra-familial similarities of granular corneal dystrophy Groenouw type I with respect to biomicroscopical appearance and symptomatology Acta Ophthalmol (Copenh) 67 1989 669 677
4. H.U. Moller Granular corneal dystrophy Groenouw type I (GRI) and Reis-Bücklers’ corneal dystrophy (R-B) one entity? Acta Ophthalmol (Copenh) 67 1989 678 684