Three Novel Mutations in the X-Linked Juvenile Retinoschisis (XLRS1) Gene in 6 Japanese Patients, 1 of Whom Had Turner’s Syndrome

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Ophthalmic Research, Vol. 35, Iss. 5, 2003-08 ,pp. : 295-300

Karger

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Identification of Novel Mutations in the XLRS1 Gene in Chinese Patients with X-linked Juvenile Retinoschisis

By Zeng Meizhen   Yi Changxian   Guo Xiangming   Jia Xiaoyun   Deng Yan   Wang Juan   Shen Huangxuan  

Current Eye Research, Vol. 32, Iss. 7-8, 2007-02 ,pp. : 685-691

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X-linked Juvenile Retinoschisis (XLRS): A Review of Genotype-Phenotype Relationships

By Kim David Y.   Mukai Shizuo  

Seminars in Ophthalmology, Vol. 28, Iss. 5-6, 2013-09 ,pp. : 392-396

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Thirty-two years follow-up of X-linked juvenile retinoschisis in a Chinese patient with RS1 mutation

By Xu Fei   Sui Ruifang   Dong Fangtian  

Ophthalmic Genetics, Vol. 33, Iss. 2, 2012-06 ,pp. : 77-82

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Severe juvenile retinoschisis associated with a 33-bps deletion in XLRS1 gene

By Shinoda Kei   Mashima Yukihiko   Ishida Susumu   Oguchi Yoshihisa  

Ophthalmic Genetics, Vol. 20, Iss. 1, 1999-03 ,pp. : 57-61

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