000 01664 a2200493 4500
005 20250514024708.0
264 0 _c20020909
008 200209s 0 0 eng d
022 _a0964-6906
024 7 _a10.1093/hmg/11.5.605
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aYang, Zhenglin
245 0 0 _aMutations in the RPGR gene cause X-linked cone dystrophy.
_h[electronic resource]
260 _bHuman molecular genetics
_cMar 2002
300 _a605-11 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAmino Acid Sequence
650 0 4 _aBase Sequence
650 0 4 _aCarrier Proteins
_xgenetics
650 0 4 _aColor Vision Defects
_xgenetics
650 0 4 _aEye Proteins
650 0 4 _aGlutamic Acid
_xmetabolism
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
_xgenetics
650 0 4 _aOpen Reading Frames
650 0 4 _aPedigree
650 0 4 _aPhotophobia
_xgenetics
650 0 4 _aRetinal Cone Photoreceptor Cells
_xphysiopathology
650 0 4 _aRetinal Degeneration
_xgenetics
650 0 4 _aSequence Deletion
650 0 4 _aVisual Fields
650 0 4 _aX Chromosome
700 1 _aPeachey, Neal S
700 1 _aMoshfeghi, Darius M
700 1 _aThirumalaichary, Sukanya
700 1 _aChorich, Lou
700 1 _aShugart, Yin Y
700 1 _aFan, Keke
700 1 _aZhang, Kang
773 0 _tHuman molecular genetics
_gvol. 11
_gno. 5
_gp. 605-11
856 4 0 _uhttps://doi.org/10.1093/hmg/11.5.605
_zAvailable from publisher's website
999 _c11782282
_d11782282