| 000 | 01485 a2200421 4500 | ||
|---|---|---|---|
| 005 | 20250516055126.0 | ||
| 264 | 0 | _c20130821 | |
| 008 | 201308s 0 0 eng d | ||
| 022 | _a1744-5094 | ||
| 024 | 7 |
_a10.3109/13816810.2011.610862 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKasbekar, Shivani A | |
| 245 | 0 | 0 |
_aCorneal endothelial dysfunction in Pearson syndrome. _h[electronic resource] |
| 260 |
_bOphthalmic genetics _c |
||
| 300 |
_a55-7 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAcyl-CoA Dehydrogenase, Long-Chain _xdeficiency |
| 650 | 0 | 4 |
_aBlepharoptosis _xdiagnosis |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aCongenital Bone Marrow Failure Syndromes |
| 650 | 0 | 4 |
_aCorneal Edema _xdiagnosis |
| 650 | 0 | 4 |
_aDNA, Mitochondrial _xgenetics |
| 650 | 0 | 4 |
_aEndothelium, Corneal _xpathology |
| 650 | 0 | 4 | _aFatal Outcome |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aLipid Metabolism, Inborn Errors _xcomplications |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMitochondrial Diseases _xcomplications |
| 650 | 0 | 4 |
_aMuscular Diseases _xcomplications |
| 650 | 0 | 4 |
_aOphthalmoplegia _xdiagnosis |
| 650 | 0 | 4 |
_aRetinitis Pigmentosa _xdiagnosis |
| 700 | 1 | _aGonzalez-Martin, Jose A | |
| 700 | 1 | _aShafiq, Ayad E | |
| 700 | 1 | _aChandna, Arvind | |
| 700 | 1 | _aWilloughby, Colin E | |
| 773 | 0 |
_tOphthalmic genetics _gvol. 34 _gno. 1-2 _gp. 55-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.3109/13816810.2011.610862 _zAvailable from publisher's website |
| 999 |
_c21174815 _d21174815 |
||