2Boycott KM, Pearce WG, Musarella MA, et al. Evidence for genetic heterogeneity in X-linked congenital stationary night blindness. Am J Hum Genet, 1998,62:865-875.
3Bech-Hansen NT, Naylor MJ, Maybaum TA, et al. Loss-of-functionmutations in a calcium-channel alpha-l-subunit gene in Xpll. 23 cause incomplete X-linked congenital stationary night blindness. Nat Genet, 1998,19 : 264-267.
4Strom TM, Nyakatura G, Apfelstedt-SyllaE, et al. An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness. Nat Genet, 1998,19 : 260-263.
5Boycott KM, Pearce WG, Bech-Hansen NT. Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F. Can J Ophthalmol,2000,35:204-213.
6Yong RS, Chaparro A, Price J, et al. Oscillatory potentials of Xlinked carriers of congenital stationary night blindness ( I-CSNB ).Invest Ophthalmol Vis Sci, 1989, 30: 806-812.
7Rigaudiere F, Roux C, Lachapelle p, et al. ERGs in female carriers of incomplete congenital stationary night blindness. Doc Ophthalmol,2003, 107: 203-212.
8Sieving PA. Photopic ON- and Off-pathway abnormalities in retinal dystrophies. Trans Am Ophthahnol, 1993, 91.701-773.
9Langrova H,Gamer D,Friedberg C,et al.Abnormalities of the long flash ERG in congetnital stationary aight blindness of the SchubertBomschein. Vis Res, 2002, 42 : 1475-1483.
10Musarella MA, Weleber BG, Murphey WH, et al. Assignment of the gene for complete X-linked congenital stationary night blindness( CSNB1 ) to human chromosome Xp11.3. Genomics, 1989,5 : 727-737.
