Progress of gene research on autosomal recessive retinitis pigmentosa
Retinal pigmentosa(RP)is a hereditary blinding retinal disease whose pathogenesis is not fully understand. It is characterized by night blindness, progressive narrowing visual field and vision decreased. Bone spicule-shaped pigment,retinal vessel attenuation and pallor optic disc can be seen at the...
Main Authors: | Rui Wang, Ming Jin |
---|---|
Format: | Article |
Language: | English |
Published: |
Press of International Journal of Ophthalmology (IJO PRESS)
2019-12-01
|
Series: | Guoji Yanke Zazhi |
Subjects: | |
Online Access: | http://ies.ijo.cn/cn_publish/2019/12/201912013.pdf |
Similar Items
-
Comparison of structural progression between ciliopathy and non-ciliopathy associated with autosomal recessive retinitis pigmentosa
by: Vitor K. L. Takahashi, et al.
Published: (2019-08-01) -
Rhodopsin mutations are scarcely implicated in autosomal recessive retinitis pigmentosa: A preliminary study of Egyptian retinitis pigmentosa patients
by: Reem Mebed, et al.
Published: (2015-10-01) -
Research progress of gene therapy for retinitis pigmentosa
by: Fang-Yuan Deng, et al.
Published: (2021-07-01) -
Research progress in the treatment of retinitis pigmentosa
by: Chen Ou, et al.
Published: (2018-09-01) -
Retinitis pigmentosa genetics: A study in Indian population
by: Vinchurkar Manisha, et al.
Published: (1996-01-01)