000 | 01239 a2200361 4500 | ||
---|---|---|---|
005 | 20250515102941.0 | ||
264 | 0 | _c20080530 | |
008 | 200805s 0 0 eng d | ||
022 | _a1381-6810 | ||
024 | 7 |
_a10.1080/13816810701663543 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aKondo, Hiroyuki | |
245 | 0 | 0 |
_aSevere form of familial exudative vitreoretinopathy caused by homozygous R417Q mutation in frizzled-4 gene. _h[electronic resource] |
260 |
_bOphthalmic genetics _cDec 2007 |
||
300 |
_a220-3 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aFrizzled Receptors _xgenetics |
650 | 0 | 4 | _aHomozygote |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 |
_aReceptors, G-Protein-Coupled _xgenetics |
650 | 0 | 4 |
_aRetinal Diseases _xgenetics |
650 | 0 | 4 | _aSuppuration |
650 | 0 | 4 |
_aVitreous Body _xpathology |
700 | 1 | _aQin, Minghui | |
700 | 1 | _aTahira, Tomoko | |
700 | 1 | _aUchio, Eiichi | |
700 | 1 | _aHayashi, Kenshi | |
773 | 0 |
_tOphthalmic genetics _gvol. 28 _gno. 4 _gp. 220-3 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1080/13816810701663543 _zAvailable from publisher's website |
999 |
_c17672783 _d17672783 |