bibliographicCitation |
Koeppen K, Reuter P, Kohl S, Baumann B, Ladewig T, Wissinger B. Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3R427C and A3R563C. Eur J of Neuroscience. 2008 Apr 25;27(9):2391–401. doi: 10.1111/j.1460-9568.2008.06195.x. |