| 000 | 01812 a2200505 4500 | ||
|---|---|---|---|
| 005 | 20250518014535.0 | ||
| 264 | 0 | _c20190524 | |
| 008 | 201905s 0 0 eng d | ||
| 022 | _a1552-5783 | ||
| 024 | 7 |
_a10.1167/iovs.18-24328 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aHassall, Mark M | |
| 245 | 0 | 0 |
_aA Novel Achromatopsia Mouse Model Resulting From a Naturally Occurring Missense Change in Cngb3. _h[electronic resource] |
| 260 |
_bInvestigative ophthalmology & visual science _c12 2018 |
||
| 300 |
_a6102-6110 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 |
_aColor Vision Defects _xgenetics |
| 650 | 0 | 4 |
_aCyclic Nucleotide-Gated Cation Channels _xgenetics |
| 650 | 0 | 4 |
_aDark Adaptation _xphysiology |
| 650 | 0 | 4 | _aDisease Models, Animal |
| 650 | 0 | 4 | _aElectroretinography |
| 650 | 0 | 4 |
_aExons _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenotyping Techniques |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMice |
| 650 | 0 | 4 | _aMice, Inbred C57BL |
| 650 | 0 | 4 |
_aMutation, Missense _xgenetics |
| 650 | 0 | 4 | _aOphthalmoscopy |
| 650 | 0 | 4 | _aPolymorphism, Restriction Fragment Length |
| 650 | 0 | 4 |
_aRNA, Messenger _xgenetics |
| 650 | 0 | 4 | _aReal-Time Polymerase Chain Reaction |
| 650 | 0 | 4 |
_aRetina _xphysiopathology |
| 650 | 0 | 4 |
_aRetinal Cone Photoreceptor Cells _xpathology |
| 650 | 0 | 4 | _aTomography, Optical Coherence |
| 700 | 1 | _aBarnard, Alun R | |
| 700 | 1 | _aOrlans, Harry O | |
| 700 | 1 | _aMcClements, Michelle E | |
| 700 | 1 | _aCharbel Issa, Peter | |
| 700 | 1 | _aAslam, Sher A | |
| 700 | 1 | _aMacLaren, Robert E | |
| 773 | 0 |
_tInvestigative ophthalmology & visual science _gvol. 59 _gno. 15 _gp. 6102-6110 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1167/iovs.18-24328 _zAvailable from publisher's website |
| 999 |
_c29204670 _d29204670 |
||