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RetinoGenetics : A comprehensive mutation database for genes related with inherited retinal degeneration

Stargardt disease : 659. Retinitis pigmentosa,X-linked : 417. Retinitis pigmentosa,AR : 367. Usher syndrome type II : 345. Leber congenital amaurosis : 320. Last Update : 03/23/2014. Welcome to the RetinoGenetics home page! Inherited retinal degeneration (IRD). A leading cause of human blindness worldwide, is exceptionally heterogeneous with clinical heterogeneity and genetic variety. For the past two decades, great progresses have been achieved in identifying disease-causing genes and mutations....

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The Eye Hospita●●●●●●●●●●●●●●●ical University

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CN

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hx●●●●●@gmail.com

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Wenzhou Medical University

XiuFeng Huang

The Eye Hospita●●●●●●●●●●●●●●●ical University

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CN

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RetinoGenetics : A comprehensive mutation database for genes related with inherited retinal degeneration | retinae.org Reviews
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Stargardt disease : 659. Retinitis pigmentosa,X-linked : 417. Retinitis pigmentosa,AR : 367. Usher syndrome type II : 345. Leber congenital amaurosis : 320. Last Update : 03/23/2014. Welcome to the RetinoGenetics home page! Inherited retinal degeneration (IRD). A leading cause of human blindness worldwide, is exceptionally heterogeneous with clinical heterogeneity and genetic variety. For the past two decades, great progresses have been achieved in identifying disease-causing genes and mutations....
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1 retinogenetics
2 browser
3 browse all
4 browse by disease
5 alagille syndrome
6 alstrom syndrome
7 bardet biedl syndrome
8 leber congenital amaurosis
9 retinitis pigmentosa
10 stargardt disease
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retinogenetics,browser,browse all,browse by disease,alagille syndrome,alstrom syndrome,bardet biedl syndrome,leber congenital amaurosis,retinitis pigmentosa,stargardt disease,usher syndrome,browse by chromosome,analysis,gene ontology analysis,ppi analysis
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RetinoGenetics : A comprehensive mutation database for genes related with inherited retinal degeneration | retinae.org Reviews

https://retinae.org

Stargardt disease : 659. Retinitis pigmentosa,X-linked : 417. Retinitis pigmentosa,AR : 367. Usher syndrome type II : 345. Leber congenital amaurosis : 320. Last Update : 03/23/2014. Welcome to the RetinoGenetics home page! Inherited retinal degeneration (IRD). A leading cause of human blindness worldwide, is exceptionally heterogeneous with clinical heterogeneity and genetic variety. For the past two decades, great progresses have been achieved in identifying disease-causing genes and mutations....

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RetinoGenetics : A comprehensive mutation database for genes related with inherited retinal degeneration

Stargardt disease : 659. Retinitis pigmentosa,X-linked : 417. Retinitis pigmentosa,AR : 367. Usher syndrome type II : 345. Leber congenital amaurosis : 320. Last Update : 03/23/2014. Welcome to the RetinoGenetics home page! Inherited retinal degeneration (IRD). A leading cause of human blindness worldwide, is exceptionally heterogeneous with clinical heterogeneity and genetic variety. For the past two decades, great progresses have been achieved in identifying disease-causing genes and mutations....

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