CRB1 mutation spectrum in inherited retinal dystrophies-Reference-Cited by-同舟云学术

CRB1 mutation spectrum in inherited retinal dystrophies

Published:2004 Issue:5 Volume:24 Page:355-369
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

den Hollander Anneke I.,Davis Jason,van der Velde-Visser Saskia D.,Zonneveld Marijke N.,Pierrottet Chiara O.,Koenekoop Robert K.,Kellner Ulrich,van den Born L. Ingeborgh,Heckenlively John R.,Hoyng Carel B.,Handford Penny A.,Roepman Ronald,Cremers Frans P.M.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference43 articles.

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2. Merging extracellular domains: fold prediction for laminin G-like and amino-terminal thrombospondin-like modules based on homology to pentraxins 1 1Edited by G. Von Heijne

3. Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa

4. Discs Lost, a Novel Multi-PDZ Domain Protein, Establishes and Maintains Epithelial Polarity

5. Zonula Adherens Formation in Caenorhabditis elegans Requires dlg-1, the Homologue of the Drosophila Gene discs large

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