Phenotype associated with an R120X nonsense mutation in the RP2 gene in a Japanese family with X-linked retinitis pigmentosa

By Mashima Yukihiko   Saga Masamichi   Akeo Kiyoshi   Oguchi Yoshihisa  

Ophthalmic Genetics, Vol. 22, Iss. 1, 2001-03 ,pp. : 43-47

Informa Healthcare

Access to resources Recommend Favorite

Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype

By Ponjavic Vesna   Andréasson Sten   Abrahamson Magnus   Ehinger Berndt   Gieser Linn   Fujita Ricardo   Swaroop Anand   Swaroop Anand  

Ophthalmic Genetics, Vol. 19, Iss. 4, 1998-12 ,pp. : 187-196

Informa Healthcare

Access to resources Recommend Favorite

Mutations in RPGR and RP2 of Chinese Patients with X-Linked Retinitis Pigmentosa

By Ji Yanli   Wang Juan   Xiao Xueshan   Li Shiqiang   Guo Xiangming   Zhang Qingjiong  

Current Eye Research, Vol. 35, Iss. 1, 2010-01 ,pp. : 73-79

Informa Healthcare

Access to resources Recommend Favorite

Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes

By Andréasson Sten   Breuer Debra K.   Eksandh Louise   Ponjavic Vesna   Frennesson Christina   Hiriyanna Suja   Filippova Elena   Yashar Beverly M.   Swaroop Anand  

Ophthalmic Genetics, Vol. 24, Iss. 4, 2003-12 ,pp. : 215-223

Informa Healthcare

Access to resources Recommend Favorite

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

Informa Healthcare

Access to resources Recommend Favorite