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 |