VSX1 mutation and corneal dystrophies

被引:10
作者
Aldave, AJ
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D O I
10.1016/j.ophtha.2004.10.017
中图分类号
R77 [眼科学];
学科分类号
100212 ;
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页码:170 / 171
页数:2
相关论文
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[1]  
ALDAVE A, IN PRESS CORNEA
[2]   VSX1:: A gene for posterior polymorphous dystrophy and keratoconus [J].
Héon, E ;
Greenberg, A ;
Kopp, KK ;
Rootman, D ;
Vincent, AL ;
Billingsley, G ;
Priston, M ;
Dorval, KM ;
Chow, RL ;
McInnes, RR ;
Heathcote, G ;
Westall, C ;
Sutphin, JE ;
Semina, E ;
Bremner, R ;
Stone, EM .
HUMAN MOLECULAR GENETICS, 2002, 11 (09) :1029-1036
[3]   VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells [J].
Mintz-Hittner, HA ;
Semina, EV ;
Frishman, LJ ;
Prager, TC ;
Murray, JC .
OPHTHALMOLOGY, 2004, 111 (04) :828-836