Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. [electronic resource]
Producer: 20100927Description: 656-66 p. digitalISSN:- 1098-1004
- Animals
- Binding Sites -- genetics
- Disease Models, Animal
- Eye Proteins -- chemistry
- Family Health
- Frizzled Receptors -- chemistry
- Humans
- LDL-Receptor Related Proteins -- chemistry
- Low Density Lipoprotein Receptor-Related Protein-5
- Mice
- Models, Molecular
- Mutation
- Nerve Tissue Proteins -- chemistry
- Protein Structure, Secondary
- Protein Structure, Tertiary
- Receptors, G-Protein-Coupled -- chemistry
- Retinal Diseases -- genetics
- Signal Transduction
- Vitreoretinopathy, Proliferative -- genetics
- Wnt Proteins -- metabolism
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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