TY  - GEN
AU  - Møller,H U
AU  - Ridgway,A E
TI  - Granular corneal dystrophy Groenouw type I. A report of a probable homozygous patient
SN  - 0001-639X
PY  - 1990///0614
KW  - Corneal Dystrophies, Hereditary
KW  - genetics
KW  - Corneal Opacity
KW  - pathology
KW  - Corneal Transplantation
KW  - Female
KW  - Homozygote
KW  - Humans
KW  - Infant
KW  - Male
KW  - Middle Aged
KW  - Pedigree
KW  - Visual Acuity
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1111/j.1755-3768.1990.tb01658.x
ER  -