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Molecular pathogenesis of achromatopsia associated with mutations in the cone cyclic nucleotide-gated channel CNGA3 subunit.
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Molecular pathogenesis of achromatopsia associated with mutations in the cone cyclic nucleotide-gated channel CNGA3 subunit.
Molecular pathogenesis of achromatopsia associated with mutations in the cone cyclic nucleotide-gated channel CNGA3 subunit. Adv Exp Med Biol. 2010; 664:245-53.
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PubMed
subject areas
Amino Acid Substitution
Amino Acid Substitution
Animals
Animals
Color Vision Defects
Color Vision Defects
Cyclic Nucleotide-Gated Cation Channels
Cyclic Nucleotide-Gated Cation Channels
Genetic Predisposition to Disease
Genetic Predisposition to Disease
HEK293 Cells
HEK293 Cells
Humans
Humans
Ion Channel Gating
Ion Channel Gating
Mice
Mice
Mutant Proteins
Mutant Proteins
Mutation
Mutation
Protein Subunits
Protein Subunits
Protein Transport
Protein Transport
Retinal Cone Photoreceptor Cells
Retinal Cone Photoreceptor Cells
authors with profiles
Xi-Qin Ding