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Summary Expression Phenotypes Gene Literature (4) GO Terms (3) Nucleotides (129) Proteins (57) Interactants (63) Wiki
XB-GENEPAGE-1000809

Papers associated with abca4



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TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa., Bocquet B, Borday C, Erkilic N, Mamaeva D, Donval A, Masson C, Parain K, Kaminska K, Quinodoz M, Perea-Romero I, Garcia-Garcia G, Jimenez-Medina C, Boukhaddaoui H, Coget A, Leboucq N, Calzetti G, Gandolfi S, Percesepe A, Barili V, Uliana V, Delsante M, Bozzetti F, Scholl HP, Corton M, Ayuso C, Millan JM, Rivolta C, Meunier I, Perron M, Kalatzis V., JCI Insight. November 8, 2023; 8 (21):                                               


Maximizing CRISPR/Cas9 phenotype penetrance applying predictive modeling of editing outcomes in Xenopus and zebrafish embryos., Naert T, Tulkens D, Edwards NA, Carron M, Shaidani NI, Wlizla M, Boel A, Demuynck S, Horb ME, Coucke P, Willaert A, Zorn AM, Vleminckx K, Vleminckx K., Sci Rep. September 4, 2020; 10 (1): 14662.                      


ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies., Wiszniewski W, Zaremba CM, Yatsenko AN, Jamrich M, Wensel TG, Lewis RA, Lupski JR., Hum Mol Genet. October 1, 2005; 14 (19): 2769-78.        


Evolution of ABCA4 proteins in vertebrates., Yatsenko AN, Wiszniewski W, Zaremba CM, Jamrich M, Lupski JR., J Mol Evol. January 1, 2005; 60 (1): 72-80.

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