hexagon 发表于 2025-3-21 18:34:56

书目名称Retinal Dystrophy Gene Atlas影响因子(影响力)<br>        http://impactfactor.cn/if/?ISSN=BK0829223<br><br>        <br><br>书目名称Retinal Dystrophy Gene Atlas影响因子(影响力)学科排名<br>        http://impactfactor.cn/ifr/?ISSN=BK0829223<br><br>        <br><br>书目名称Retinal Dystrophy Gene Atlas网络公开度<br>        http://impactfactor.cn/at/?ISSN=BK0829223<br><br>        <br><br>书目名称Retinal Dystrophy Gene Atlas网络公开度学科排名<br>        http://impactfactor.cn/atr/?ISSN=BK0829223<br><br>        <br><br>书目名称Retinal Dystrophy Gene Atlas被引频次<br>        http://impactfactor.cn/tc/?ISSN=BK0829223<br><br>        <br><br>书目名称Retinal Dystrophy Gene Atlas被引频次学科排名<br>        http://impactfactor.cn/tcr/?ISSN=BK0829223<br><br>        <br><br>书目名称Retinal Dystrophy Gene Atlas年度引用<br>        http://impactfactor.cn/ii/?ISSN=BK0829223<br><br>        <br><br>书目名称Retinal Dystrophy Gene Atlas年度引用学科排名<br>        http://impactfactor.cn/iir/?ISSN=BK0829223<br><br>        <br><br>书目名称Retinal Dystrophy Gene Atlas读者反馈<br>        http://impactfactor.cn/5y/?ISSN=BK0829223<br><br>        <br><br>书目名称Retinal Dystrophy Gene Atlas读者反馈学科排名<br>        http://impactfactor.cn/5yr/?ISSN=BK0829223<br><br>        <br><br>

organism 发表于 2025-3-21 22:45:16

,,eveloping and adult photoreceptor layer. It has also been shown to affect photoreceptor function as well as signal transduction through its mediation of cone PDE6 and RetGC1, respectively . Mutations in . cause recessive Leber congenital amaurosis (LCA) and juvenile-onset rod-cone dystrophy, dominant cone-rod dystrophy has also been reported.

Munificent 发表于 2025-3-22 01:41:30

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

conservative 发表于 2025-3-22 04:34:48

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Anticoagulants 发表于 2025-3-22 11:53:01

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

Hypopnea 发表于 2025-3-22 14:34:34

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边缘 发表于 2025-3-22 17:04:04

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感情脆弱 发表于 2025-3-23 01:09:05

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Acetabulum 发表于 2025-3-23 05:00:45

https://doi.org/10.1007/978-3-319-10867-4Autosomal Dominant Inheritance; Autosomal Recessive Inheritance; Linked Inheritance; Retinal Dystrophy;

forecast 发表于 2025-3-23 07:22:09

978-3-030-13234-7Springer International Publishing AG, part of Springer Nature 2018
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查看完整版本: Titlebook: Retinal Dystrophy Gene Atlas; Sarwar Zahid,Kari Branham,Thiran Jayasundera Book 2018 Springer International Publishing AG, part of Springe