000 | 01440 a2200469 4500 | ||
---|---|---|---|
005 | 20250516231605.0 | ||
264 | 0 | _c20150521 | |
008 | 201505s 0 0 eng d | ||
022 | _a1476-5454 | ||
024 | 7 |
_a10.1038/eye.2014.196 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aHuang, Y | |
245 | 0 | 0 |
_aA novel deletion mutation in RS1 gene caused X-linked juvenile retinoschisis in a Chinese family. _h[electronic resource] |
260 |
_bEye (London, England) _cNov 2014 |
||
300 |
_a1364-9 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aAsian People _xgenetics |
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aChina |
650 | 0 | 4 | _aDNA Mutational Analysis |
650 | 0 | 4 |
_aEye Proteins _xgenetics |
650 | 0 | 4 | _aFluorescein Angiography |
650 | 0 | 4 | _aFrameshift Mutation |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 | _aPolymerase Chain Reaction |
650 | 0 | 4 |
_aRetinoschisis _xgenetics |
650 | 0 | 4 | _aSequence Deletion |
650 | 0 | 4 | _aTomography, Optical Coherence |
650 | 0 | 4 | _aVisual Acuity |
700 | 1 | _aMei, L | |
700 | 1 | _aGui, B | |
700 | 1 | _aSu, W | |
700 | 1 | _aLiang, D | |
700 | 1 | _aWu, L | |
700 | 1 | _aPan, Q | |
773 | 0 |
_tEye (London, England) _gvol. 28 _gno. 11 _gp. 1364-9 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1038/eye.2014.196 _zAvailable from publisher's website |
999 |
_c24140773 _d24140773 |