| 000 | 01815 a2200553 4500 | ||
|---|---|---|---|
| 005 | 20250516224740.0 | ||
| 264 | 0 | _c20150123 | |
| 008 | 201501s 0 0 eng d | ||
| 022 | _a2168-6173 | ||
| 024 | 7 |
_a10.1001/jamaophthalmol.2014.2343 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aHull, Sarah | |
| 245 | 0 | 0 |
_aClinical and molecular characterization of enhanced S-cone syndrome in children. _h[electronic resource] |
| 260 |
_bJAMA ophthalmology _cNov 2014 |
||
| 300 |
_a1341-9 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aElectroretinography |
| 650 | 0 | 4 |
_aEye Diseases, Hereditary _xdiagnosis |
| 650 | 0 | 4 |
_aEye Proteins _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFluorescein Angiography |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMolecular Biology |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aNight Blindness _xdiagnosis |
| 650 | 0 | 4 |
_aOrphan Nuclear Receptors _xgenetics |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymerase Chain Reaction |
| 650 | 0 | 4 |
_aRetinal Degeneration _xdiagnosis |
| 650 | 0 | 4 | _aTomography, Optical Coherence |
| 650 | 0 | 4 |
_aVision Disorders _xdiagnosis |
| 650 | 0 | 4 |
_aVisual Acuity _xphysiology |
| 700 | 1 | _aArno, Gavin | |
| 700 | 1 | _aSergouniotis, Panagiotis I | |
| 700 | 1 | _aTiffin, Peter | |
| 700 | 1 | _aBorman, Arundhati Dev | |
| 700 | 1 | _aChandra, Aman | |
| 700 | 1 | _aRobson, Anthony G | |
| 700 | 1 | _aHolder, Graham E | |
| 700 | 1 | _aWebster, Andrew R | |
| 700 | 1 | _aMoore, Anthony T | |
| 773 | 0 |
_tJAMA ophthalmology _gvol. 132 _gno. 11 _gp. 1341-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1001/jamaophthalmol.2014.2343 _zAvailable from publisher's website |
| 999 |
_c24057955 _d24057955 |
||