Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOX

European Journal of Human Genetics

Volumn 4, Issue 4, 1996, Pages 214-218

  Korvatska, Elena ^b   Munier, F L ^a   Zografos, L ^a   Ahmad, F ^a   Faggioni, R ^a   Dolivo Beuret, A ^a   Pescia, G ^a   Schorderet, D F ^a  

^a LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^b NONE

Author keywords

Chromosome 5; Corneal dystrophy; Groenouw type I; Lattice type I; Linkage analysis

Indexed keywords

ARTICLE; CHROMOSOME 5Q; CHROMOSOME MAP; CORNEA DYSTROPHY; FAMILY STUDY; GENE LOCUS; GENETIC LINKAGE; HAPLOTYPE; PRIORITY JOURNAL; SWITZERLAND;

EID: 0029819807     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1159/000472201     Document Type: Article

References (2)

1. Rodrigues MM, Streeten BW, Krachmer JH, Laibson PR, Salem N, Passoneau J, Chock S: Microfibrillar protein and phospholipid in granular corneal dystrophy. Arch Ophthalmol 1983;101:802-810.
2. Rodrigues MM, Kruth HS, Rajagopalan S, Jones K: Unesterified cholesterol in granular, lattice, and macular dystrophies. Am J Ophthalmol 1993;115:112-114.