Titlebook: Retinal Dystrophy Gene Atlas; Sarwar Zahid,Kari Branham,Thiran Jayasundera Book 2018 Springer International Publishing AG, part of Springe

BALK

保守党

,,ponsible for rod-cone (86.9%) and cone-rod (13.1%) dystrophies [2] and for syndromic features associated with Bardet-Biedl syndrome (BBS). . mutations may also cause isolated retinitis pigmentosa (RP) [3, 4].

陈腐思想

管理员

,,kely function in membrane trafficking to the primary cilium [1]. Mutations are responsible for rod-cone (86.9%) and cone-rod (13.1%) dystrophies [2] and for syndromic features associated with Bardet-Biedl Syndrome.

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吸引人的花招

,,kely function in membrane trafficking to the primary cilium [1]. . in particular has a possible role in regulating light-dependent translocation of arrestin1, which moves between photoreceptor inner and outer segments according to light conditions [2]. Mutations are responsible for rod-cone (86.9%)

不妥协

,,kely function in membrane trafficking to the primary cilium [1]. Mutations are responsible for rod-cone (86.9%) and cone-rod (13.1%) dystrophies [2] and for syndromic features associated with BBS. Ocular features vary widely, however. In a Chinese family with . mutations, patients were found to have

谷物

,,acular vitelliform dystrophy (AOFVD), autosomal dominant vitreoretinochoroidopathy (ADVIRC), microcornea, rod-cone dystrophy, cataract, posterior staphyloma (MRCS) syndrome, and autosomal recessive bestrophinopathy (ARB) [1].

EWE

,,-linked and have been reported to cause 55% of congenital stationary night blindness (CSNB). They have also been associated with cone-rod dystrophy, Aland Eye Disease, and retinal and optic disc atrophy [2–7].

initiate

,,restin1, which moves between photoreceptor inner and outer segments according to light conditions [2]. Mutations are responsible for rod-cone (86.9%) and cone-rod (13.1%) dystrophies [3] and for syndromic features associated with BBS.