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ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculatureDisruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophyThe DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1MPP1 links the Usher protein network and the Crumbs protein complex in the retinaOFD1 is mutated in X-linked Joubert syndrome and interacts with LCA5-encoded lebercilinIdentification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type IIMutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunctionKIAA0556 is a novel ciliary basal body component mutated in Joubert syndromeScaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cellsNINL and DZANK1 Co-function in Vesicle Transport and Are Essential for Photoreceptor Development in Zebrafish
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Erwin van Wijk
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Erwin van Wijk
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Erwin van Wijk
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Erwin van Wijk
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Erwin van Wijk
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Erwin van Wijk
@ast
Erwin van Wijk
@en
Erwin van Wijk
@es
Erwin van Wijk
@nl
Erwin van Wijk
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Erwin van Wijk
@ast
Erwin van Wijk
@en
Erwin van Wijk
@es
Erwin van Wijk
@nl
Erwin van Wijk
@sl