000 | 01522 a2200481 4500 | ||
---|---|---|---|
005 | 20250515205255.0 | ||
264 | 0 | _c20100401 | |
008 | 201004s 0 0 eng d | ||
022 | _a1744-5094 | ||
024 | 7 |
_a10.3109/13816810903452047 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aKhan, Arif O | |
245 | 0 | 0 |
_aLater retinal degeneration following childhood surgical aphakia in a family with recessive CRYAB mutation (p.R56W). _h[electronic resource] |
260 |
_bOphthalmic genetics _cMar 2010 |
||
300 |
_a30-6 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aAdult |
650 | 0 | 4 |
_aAphakia, Postcataract _xetiology |
650 | 0 | 4 |
_aCataract _xgenetics |
650 | 0 | 4 | _aCataract Extraction |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aConsanguinity |
650 | 0 | 4 | _aElectroretinography |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGenes, Recessive |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 | _aMutation, Missense |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
650 | 0 | 4 | _aProspective Studies |
650 | 0 | 4 |
_aRetinal Degeneration _xgenetics |
650 | 0 | 4 | _aVisual Acuity |
650 | 0 | 4 |
_aalpha-Crystallin B Chain _xgenetics |
700 | 1 | _aAbu Safieh, Leen | |
700 | 1 | _aAlkuraya, Fowzan S | |
700 | 1 | _aAlkurarya, Fowzan S | |
773 | 0 |
_tOphthalmic genetics _gvol. 31 _gno. 1 _gp. 30-6 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.3109/13816810903452047 _zAvailable from publisher's website |
999 |
_c19512388 _d19512388 |