000 01482 a2200457 4500
005 20250513185851.0
264 0 _c20000111
008 200001s 0 0 eng d
022 _a0007-1161
024 7 _a10.1136/bjo.83.8.914
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKlevering, B J
245 0 0 _aPhenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene.
_h[electronic resource]
260 _bThe British journal of ophthalmology
_cAug 1999
300 _a914-8 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aATP-Binding Cassette Transporters
_xgenetics
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aAged, 80 and over
650 0 4 _aConsanguinity
650 0 4 _aFemale
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
_xgenetics
650 0 4 _aNight Blindness
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aRetinal Degeneration
_xgenetics
650 0 4 _aVisual Acuity
_xgenetics
650 0 4 _aVisual Fields
_xgenetics
700 1 _avan Driel, M
700 1 _avan de Pol, D J
700 1 _aPinckers, A J
700 1 _aCremers, F P
700 1 _aHoyng, C B
773 0 _tThe British journal of ophthalmology
_gvol. 83
_gno. 8
_gp. 914-8
856 4 0 _uhttps://doi.org/10.1136/bjo.83.8.914
_zAvailable from publisher's website
999 _c10371771
_d10371771