Author:
van Genderen Maria M.,Bijveld Mieke M.C.,Claassen Yvonne B.,Florijn Ralph J.,Pearring Jillian N.,Meire Francoise M.,McCall Maureen A.,Riemslag Frans C.C.,Gregg Ronald G.,Bergen Arthur A.B.,Kamermans Maarten
Subject
Genetics(clinical),Genetics
Reference24 articles.
1. Congenital stationary night blindness with negative electroretinogram. A new classification;Miyake;Arch. Ophthalmol.,1986
2. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness;Bech-Hansen;Nat. Genet.,2000
3. Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene;Scholl;Invest. Ophthalmol. Vis. Sci.,2001
4. Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness;Zeitz;Mol. Vis.,2005
5. Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6;Dryja;Proc. Natl. Acad. Sci. USA,2005
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