| 000 | 01116 a2200337 4500 | ||
|---|---|---|---|
| 005 | 20250511234448.0 | ||
| 264 | 0 | _c19900614 | |
| 008 | 199006s 0 0 eng d | ||
| 022 | _a0001-639X | ||
| 024 | 7 |
_a10.1111/j.1755-3768.1990.tb01658.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMøller, H U | |
| 245 | 0 | 0 |
_aGranular corneal dystrophy Groenouw type I. A report of a probable homozygous patient. _h[electronic resource] |
| 260 |
_bActa ophthalmologica _cFeb 1990 |
||
| 300 |
_a97-101 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aCorneal Dystrophies, Hereditary _xgenetics |
| 650 | 0 | 4 |
_aCorneal Opacity _xpathology |
| 650 | 0 | 4 | _aCorneal Transplantation |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aVisual Acuity |
| 700 | 1 | _aRidgway, A E | |
| 773 | 0 |
_tActa ophthalmologica _gvol. 68 _gno. 1 _gp. 97-101 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1755-3768.1990.tb01658.x _zAvailable from publisher's website |
| 999 |
_c2343019 _d2343019 |
||