Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein

By Isosomppi J.  

Human Molecular Genetics, Vol. 11, Iss. 8, 2002-04 ,pp. : 885-891

Oxford University Press

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A function retained by the common mutant CLN3 protein is responsible for the late onset of juvenile neuronal ceroid lipofuscinosis

By Kitzmller Claudia   Haines Rebecca L.   Codlin Sandra   Cutler Daniel F.   Mole Sara E.  

Human Molecular Genetics, Vol. 17, Iss. 2, 2008-01 ,pp. : 303-312

Oxford University Press

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Mutations in the palmitoyl-protein thioesterase gene ( PPT ; CLN1 ) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposits

By Taschner P.E.M.  

Human Molecular Genetics, Vol. 7, Iss. 2, 1998-02 ,pp. : 291-297

Oxford University Press

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A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging

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Human Molecular Genetics, Vol. 13, Iss. 23, 2004-12 ,pp. : 2893-2906

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Transcript and in silico analysis of CLN3 in juvenile neuronal ceroid lipofuscinosis and associated mouse models

By Chan Chun-Hung   Mitchison Hannah M.   Pearce David A.  

Human Molecular Genetics, Vol. 17, Iss. 21, 2008-11 ,pp. : 3332-3339

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