Literature DB >> 22183383

A novel missense mutation in both OPN1LW and OPN1MW cone opsin genes causes X-linked cone dystrophy (XLCOD5).

Jessica C Gardner1, Tom R Webb, Naheed Kanuga, Anthony G Robson, Graham E Holder, Andrew Stockman, Caterina Ripamonti, Neil D Ebenezer, Olufunmilola Ogun, Sophie Devery, Genevieve A Wright, Eamonn R Maher, Michael E Cheetham, Anthony T Moore, Michel Michaelides, Alison J Hardcastle.   

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Year:  2012        PMID: 22183383     DOI: 10.1007/978-1-4614-0631-0_76

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


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  1 in total

1.  G protein-coupled receptors participate in cytokinesis.

Authors:  Xin Zhang; Anne V Bedigian; Wenchao Wang; Ulrike S Eggert
Journal:  Cytoskeleton (Hoboken)       Date:  2012-08-28
  1 in total

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