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Biochim. Biophys. Acta · Nov 2013
ReviewBioinformatic perspectives in the neuronal ceroid lipofuscinoses.
- Stanislav Kmoch, Viktor Stránecký, Richard D Emes, and Hannah M Mitchison.
- Institute for Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague, 120 00 Prague, Czech Republic.
- Biochim. Biophys. Acta. 2013 Nov 1;1832(11):1831-41.
AbstractThe neuronal ceroid lipofuscinoses (NCLs) are a group of rare genetic diseases characterised clinically by the progressive deterioration of mental, motor and visual functions and histopathologically by the intracellular accumulation of autofluorescent lipopigment - ceroid - in affected tissues. The NCLs are clinically and genetically heterogeneous and more than 14 genetically distinct NCL subtypes have been described to date (CLN1-CLN14) (Haltia and Goebel, 2012 [1]). In this review we will chronologically summarise work which has led over the years to identification of NCL genes, and outline the potential of novel genomic techniques and related bioinformatic approaches for further genetic dissection and diagnosis of NCLs. This article is part of a Special Issue entitled: The Neuronal Ceroid Lipofuscinoses or Batten Disease.Copyright © 2013 Elsevier B.V. All rights reserved.
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