000 | 01917 a2200577 4500 | ||
---|---|---|---|
005 | 20250516140146.0 | ||
264 | 0 | _c20130514 | |
008 | 201305s 0 0 eng d | ||
022 | _a1552-5783 | ||
024 | 7 |
_a10.1167/iovs.12-10967 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aChen, Xuejuan | |
245 | 0 | 0 |
_aTargeted sequencing of 179 genes associated with hereditary retinal dystrophies and 10 candidate genes identifies novel and known mutations in patients with various retinal diseases. _h[electronic resource] |
260 |
_bInvestigative ophthalmology & visual science _cMar 2013 |
||
300 |
_a2186-97 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aAsian People _xgenetics |
650 | 0 | 4 | _aChina |
650 | 0 | 4 | _aCohort Studies |
650 | 0 | 4 |
_aDNA Mutational Analysis _xmethods |
650 | 0 | 4 | _aGenetic Predisposition to Disease |
650 | 0 | 4 |
_aHigh-Throughput Nucleotide Sequencing _xmethods |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMicroarray Analysis |
650 | 0 | 4 |
_aMutation _xgenetics |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 |
_aRetinal Dystrophies _xcongenital |
700 | 1 | _aZhao, Kanxing | |
700 | 1 | _aSheng, Xunlun | |
700 | 1 | _aLi, Yang | |
700 | 1 | _aGao, Xiang | |
700 | 1 | _aZhang, Xiumei | |
700 | 1 | _aKang, Xiaoli | |
700 | 1 | _aPan, Xinyuan | |
700 | 1 | _aLiu, Yuan | |
700 | 1 | _aJiang, Chao | |
700 | 1 | _aShi, Houxia | |
700 | 1 | _aChen, Xue | |
700 | 1 | _aRong, Weining | |
700 | 1 | _aChen, Li Jia | |
700 | 1 | _aLai, Tim Yuk Yau | |
700 | 1 | _aLiu, Yani | |
700 | 1 | _aWang, Xiuying | |
700 | 1 | _aYuan, Songtao | |
700 | 1 | _aLiu, Qinghuai | |
700 | 1 | _aVollrath, Douglas | |
700 | 1 | _aPang, Chi Pui | |
700 | 1 | _aZhao, Chen | |
773 | 0 |
_tInvestigative ophthalmology & visual science _gvol. 54 _gno. 3 _gp. 2186-97 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1167/iovs.12-10967 _zAvailable from publisher's website |
999 |
_c22555299 _d22555299 |