000 01542 a2200517 4500
005 20250517003948.0
264 0 _c20150414
008 201504s 0 0 eng d
022 _a1549-4713
024 7 _a10.1016/j.ophtha.2014.07.057
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aAli, Shahbaz
245 0 0 _aPhenotypic variability associated with the D226N allele of IMPDH1.
_h[electronic resource]
260 _bOphthalmology
_cFeb 2015
300 _a429-31 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aAlleles
650 0 4 _aChild
650 0 4 _aConsanguinity
650 0 4 _aElectroretinography
650 0 4 _aFemale
650 0 4 _aGenetic Linkage
650 0 4 _aHumans
650 0 4 _aIMP Dehydrogenase
_xgenetics
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aPhotic Stimulation
650 0 4 _aRetinitis Pigmentosa
_xdiagnosis
650 0 4 _aYoung Adult
700 1 _aKhan, Shahid Y
700 1 _aNaeem, Muhammad Asif
700 1 _aKhan, Shaheen N
700 1 _aHusnain, Tayyab
700 1 _aRiazuddin, Saima
700 1 _aAyyagari, Radha
700 1 _aRiazuddin, Sheikh
700 1 _aHejtmancik, J Fielding
700 1 _aRiazuddin, S Amer
773 0 _tOphthalmology
_gvol. 122
_gno. 2
_gp. 429-31
856 4 0 _uhttps://doi.org/10.1016/j.ophtha.2014.07.057
_zAvailable from publisher's website
999 _c24394577
_d24394577