000 01155 a2200301 4500
005 20250512061701.0
264 0 _c19870626
008 198706s 0 0 ger d
022 _a0023-2165
024 7 _a10.1055/s-2008-1050353
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWeidle, E G
245 0 0 _a[Corneal opacity as the leading symptom of hereditary lecithin-cholesterol acyltransferase (LCAT) deficiency. Case report and a review of the literature].
_h[electronic resource]
260 _bKlinische Monatsblatter fur Augenheilkunde
_cMar 1987
300 _a182-7 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAdult
650 0 4 _aCorneal Opacity
_xgenetics
650 0 4 _aCorneal Stroma
_xpathology
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aHypolipoproteinemias
_xgenetics
650 0 4 _aLecithin Cholesterol Acyltransferase Deficiency
_xgenetics
650 0 4 _aPedigree
700 1 _aLisch, W
773 0 _tKlinische Monatsblatter fur Augenheilkunde
_gvol. 190
_gno. 3
_gp. 182-7
856 4 0 _uhttps://doi.org/10.1055/s-2008-1050353
_zAvailable from publisher's website
999 _c3592251
_d3592251