Lattice corneal dystrophy [1] (multiple letters)

Ophthalmology

Volumn 107, Issue 9, 2000, Pages 1613-1614

  Schmitt Bernard, Clair Florent ^a   Claustres, Mireille ^a   Arnaud, Bernard ^a   Demaille, Jacques ^a   Argiles, Àngel ^a  

^a NONE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CASE REPORT; CLINICAL FEATURE; CORNEA DYSTROPHY; DISEASE COURSE; FAMILIAL DISEASE; FEMALE; GENE MUTATION; GENETIC SCREENING; HUMAN; LETTER; OUTPATIENT; PRIORITY JOURNAL; VISUAL ACUITY;

ADULT; CORNEAL DYSTROPHIES, HEREDITARY; DNA MUTATIONAL ANALYSIS; EXTRACELLULAR MATRIX PROTEINS; FEMALE; GENETIC SCREENING; HUMANS; MALE; MIDDLE AGED; MUTATION; NEOPLASM PROTEINS; PEDIGREE; TRANSFORMING GROWTH FACTOR BETA;

EID: 0033756220     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0161-6420(00)00055-5     Document Type: Letter

References (1)

1. H. Stewart G.C. Black D. Donnai A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophy Ophthalmology 106 1999 964 970