CRB2 acts as a modifying factor of CRB1-related retinal dystrophies in mice-Reference-Cited by-同舟云学术

CRB2 acts as a modifying factor of CRB1-related retinal dystrophies in mice

Published:2014-02-23 Issue:14 Volume:23 Page:3759-3771
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Pellissier Lucie P.,Lundvig Ditte M. S.,Tanimoto Naoyuki,Klooster Jan,Vos Rogier M.,Richard Fabrice,Sothilingam Vithiyanjali,Garcia Garrido Marina,Le Bivic André,Seeliger Mathias W.,Wijnholds Jan

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/23/14/3759/13917142/ddu089.pdf

Reference44 articles.

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2. Leber congenital amaurosis: genes, proteins and disease mechanisms;den Hollander;Prog. Retin. Eye Res.,2008

3. CRB1 mutation spectrum in inherited retinal dystrophies;den Hollander;Hum. Mutat.,2004

4. Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12);den Hollander;Nat. Genet.,1999

5. CRB1 mutations in inherited retinal dystrophies;Bujakowska;Hum. Mutat.,2012

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