CRB1-Associated Retinal Dystrophies: A Prospective Natural History Study in Anticipation of Future Clinical Trials-Reference-Cited by-同舟云学术

CRB1-Associated Retinal Dystrophies: A Prospective Natural History Study in Anticipation of Future Clinical Trials

Published:2022-02 Issue: Volume:234 Page:37-48
ISSN:0002-9394
Container-title:American Journal of Ophthalmology
language:en
Short-container-title:American Journal of Ophthalmology

Author:

Nguyen Xuan-Thanh-An^ORCID,Talib Mays,van Schooneveld Mary J.,Wijnholds Jan^ORCID,van Genderen Maria M.^ORCID,Schalij-Delfos Nicoline E.,Klaver Caroline C.W.,Talsma Herman E.^ORCID,Fiocco Marta,Florijn Ralph J.,ten Brink Jacoline B.^ORCID,Cremers Frans P.M.,Meester-Smoor Magda A.,van den Born L. Ingeborgh,Hoyng Carel B.,Thiadens Alberta A.H.J.^ORCID,Bergen Arthur A.,Boon Camiel J.F.^ORCID

Publisher

Elsevier BV

Subject

Ophthalmology

Reference58 articles.

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3. Mutations in the CRB1 gene cause Leber congenital amaurosis;Lotery;Arch Opthalmol,2001

4. Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene;den Hollander;Am J Hum Genet,2001

5. Non-syndromic retinitis pigmentosa;Verbakel;Prog Retin Eye Res,2018

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