NR2E3mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP)-Reference-Cited by-同舟云学术

NR2E3mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP)

Published:2009-11 Issue:11 Volume:30 Page:1475-1485
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Schorderet Daniel F.,Escher Pascal

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference76 articles.

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3. The SWISS-MODEL Workspace: a web-based environment for protein structure homology modelling;Arnold;Bioinformatics,2006

4. Phenotypic variation in enhanced S-cone syndrome;Audo;Invest Ophthalmol Vis Sci,2008

5. The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patients;Bandah;Arch Ophthalmol,2009

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