TY  - GEN
AU  - Weidle,E G
AU  - Lisch,W
TI  - [Corneal opacity as the leading symptom of hereditary lecithin-cholesterol acyltransferase (LCAT) deficiency. Case report and a review of the literature]
SN  - 0023-2165
PY  - 1987///0626
KW  - Adult
KW  - Corneal Opacity
KW  - genetics
KW  - Corneal Stroma
KW  - pathology
KW  - Female
KW  - Humans
KW  - Hypolipoproteinemias
KW  - Lecithin Cholesterol Acyltransferase Deficiency
KW  - Pedigree
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1055/s-2008-1050353
ER  -