1Miki Hiraoka,Michael T. Trese,B. S. Shastry. Intragenic polymorphic missense mutations in the XLRS1 gene in families with juvenile X-linked retinoschisis[J] 1999,Human Genetics(6):526~527
2Y. Hotta,Keiko Fujiki,Mutsuko Hayakawa,Takashi Ohta,Takuro Fujimaki,Kouichi Tamaki,Toshiyuki Yokoyama,Atsushi Kanai,Akito Hirakata,Tetsuo Hida,Sachiko Nishina,Noriyuki Azuma. Japanese juvenile retinoschisis is caused by mutations of the XLRS1 gene[J] 1998,Human Genetics(2):142~144
3Madjarov B,Hilton GF.Brinton DA,et al.A new classification of the retinoschises.Retina,1995,15(4):282-285.
4Avinash Tantri,Vrabee TR,Andrew Cu-Unjieng,et al.X-Linked Retinoschisis:A clinical and molecular genetic review[J].Survey of Ophthalmol,2004,49(2):214-226.
5Duetman AF.Sex-linked juvenile retinoschisis.The hereditary dystrophies of the posterior pole of the eye[M].Netherlands:Van Gorcum,1971.48-98.
6Madhavendra Bhandafi, Rajni Rajah, Tandava Kristman, et al. Morphological and functional correlates in Goldmann-Faw'e syndrome: a case series[J]. Korean J Ophthahnol, 2012, 26(2): 143-146. DOI: 10. 3341/kjo. 2012.26.2. 143.
7Theodossiadis PG, Koutsandrea C, Kollia AC, et al. Optical coherence tomography in the study of the Goldmann-Favre syndronle [J]. Am J Ophlhahnol, 2000, 129(4): 542- 544.
8Pachydaki SI, Klaver CC, Barbazetto IA, et al. Phenolypic features of patients with NR2E3 mutations[J]. Arch Ophthalmol, 2009, 127(1): 71-75.
9Peyman GA, Fishman GA, Sanders DR, et al. Histopathology of Goldmann-Favre syndrome obtained by full-thickness eye- wall biopsy[J]. Ann Ophthalmol, 1977, 9(4): 479-484.
10Udar N, Small K, Chalukya M, et al. Developmental or degenerative--NR2E3 gene mutations in two patients with enhanced S cone syndrome[J]. Mol Vis, 2011, 17: 519-525.