Gelatino-lattice corneal dystrophy: Clinical features and mutational analysis

American Journal of Ophthalmology

Volumn 129, Issue 5, 2000, Pages 665-666

  Nakamura, Takahiro ^a   Nishida, Kohji ^a   Dota, Atsuyoshi ^a   Adachi, Wakako ^a   Yamamoto, Shuji ^b   Maeda, Naoyuki ^b   Okada, Masaki ^b   Kinoshita, Shigeru ^a  

^a KYOTO PREFECTURAL UNIVERSITY OF MEDICINE   (Japan)

^b OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; NUCLEOTIDE;

ADULT; CLINICAL ARTICLE; CLINICAL FEATURE; CORNEA DYSTROPHY; DISEASE CLASSIFICATION; EXON; FEMALE; GENE AMPLIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; HUMAN; JAPAN; MALE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SHORT SURVEY;

EID: 0034066271     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(00)00369-X     Document Type: Article

References (5)

1. Klintworth G.K. Lattice corneal dystrophy an inherited variety of amyloidosis restricted to the cornea . Am J Pathol. 50:1967;371-399.
2. Nagataki S., Tanishima T., Sakamoto T., et al. A case of primary gelatinous drop-like corneal dystrophy. Jpn J Ophthalmol. 16:1972;107-116.
3. Stone E.M., Mathers W.D., Rosenwasser G.O.D., et al. Three autosomal dominant corneal dystrophies map to chromosome 5q. Nat Genet. 6:1994;47-51.
4. Munier F.L., Korvatska E., Djemai A., et al. Kerato-epithelin mutations in four 5q31-linked corneal dystrophies. Nat Genet. 15:1997;247-251.
5. Tsujikawa M., Kurahashi H., Tanaka T., et al. Identification of the gene responsible for gelatinous drop-like corneal dystrophy. Nat Genet. 21:1999;420-424.