Citations for
1ATP13A2, CLN12
Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited α-synuclein accumulation and age-dependent sensorimotor deficits.
Schultheis PJ, Fleming SM, Clippinger AK, Lewis J, Tsunemi T, Giasson B, Dickson DW, Mazzulli JR, Bardgett ME, Haik KL, Ekhator O, Chava AK, Howard J, Gannon M, Hoffman E, Chen Y, Prasad V, Linn SC, Tamargo RJ, Westbroek W, Sidransky E, Krainc D, Shull GE.
Hum Mol Genet 22(10):2067-82. doi: 10.1093/hmg/ddt057. Epub 2013 Feb 7. 2013
2ATP13A2, CLN12
Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis.
Bras J, Verloes A, Schneider SA, Mole SE, Guerreiro RJ.
Hum Mol Genet 21(12):2646-50. doi: 10.1093/hmg/dds089. Epub 2012 Mar 2. 2012