Common exonic missense variants in the C2 domain of the human KIBRA protein modify lipid binding and cognitive performance

The human KIBRA gene has been linked to human cognition through a lead intronic single-nucleotide polymorphism (SNP; rs17070145) that is associated with episodic memory performance and the risk to develop Alzheimer's disease. However, it remains unknown how this relates to the function of the K...

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Autors principals: Duning, K, Wennmann, D O, Bokemeyer, A, Reissner, C, Wersching, H, Thomas, C, Buschert, J, Guske, K, Franzke, V, Flöel, A, Lohmann, H, Knecht, S, Brand, S-M, Pöter, M, Rescher, U, Missler, M, Seelheim, P, Pröpper, C, Boeckers, T M, Makuch, L, Huganir, R, Weide, T, Brand, E, Pavenstädt, H, Kremerskothen, J
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group 2013
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3693407/
https://ncbi.nlm.nih.gov/pubmed/23778582
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/tp.2013.49
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