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A lysosomal enigma CLN5 and its significance in understanding neuronal ceroid lipofuscinosis |
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| Authors: | Basak I Wicky H E McDonald K O Xu J B Palmer J E Best H L Lefrancois S Lee S Y Schoderboeck L Hughes S M |
| Institution: | 1.Neurodegenerative and Lysosomal Disease Laboratory, Department of Biochemistry, School of Biomedical Sciences, Brain Health Research Centre, University of Otago, 710 Cumberland Street, Dunedin, 9016, New Zealand ;2.School of Biosciences, Cardiff University, Sir Martin Evans Building, Museum Avenue, Wales, CF10 3AX, United Kingdom ;3.Centre INRS-Institut Armand-Frappier, INRS, Laval, H7V 1B7, Canada ;4.Department of Anatomy and Cell Biology, McGill University, Montreal, H3A 2B2, Canada ;5.Department of Biochemistry and Molecular Biology, University of Kansas Medical Center, Kansas City, KS, 66160, USA ; |
| Abstract: | Cellular and Molecular Life Sciences - Neuronal Ceroid Lipofuscinosis (NCL), also known as Batten disease, is an incurable childhood brain disease. The thirteen forms of NCL are caused by mutations... |
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