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SCIENTIFIC REPORTS, ISSN 2045-2322, 07/2019, Volume 9, Issue 1, pp. 9891 - 8
Journal Article
ORPHANET JOURNAL OF RARE DISEASES, ISSN 1750-1172, 01/2019, Volume 14, Issue 1, pp. 19 - 19
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2019, Volume 9, Issue 1, pp. 151 - 12
Neuronal ceroid lipofuscinoses (NCLs) are a group of inherited neurodegenerative lysosomal storage disorders. CLN5 deficiency causes a subtype of NCL, referred... 
STORAGE | WILD-TYPE | A-BETA COMPONENT | MESSENGER-RNA | MONITORING AUTOPHAGY | PRESYNAPTIC PROTEIN | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | BATTEN-DISEASE | EXPRESSION | PARKINSONS-DISEASE | Pathogenicity | Proteins | Fibroblasts | Lysosomes | Lysosomal storage diseases | Neuronal ceroid lipofuscinosis | Synuclein | Lysosomal protein | Autophagy | Phagocytosis
Journal Article
Clinical Trials, ISSN 1740-7745, 10/2019, Volume 16, Issue 5, pp. 555 - 560
Journal Article
BBA - Biomembranes, ISSN 0005-2736, 10/2019, Volume 1861, Issue 10, pp. 182993 - 182993
Mutations in the gene (PARK9, CLN12, OMIM ) were initially associated with a form of Parkinson's Disease (PD) known as Kufor Rakeb Syndrome (KRS). However, the... 
P type ATPase | Parkinson's disease | Neuronal ceroid lipofuscinosis | Lipid homeostasis | P5B–ATP13A2 | Phospholipidosis | Index Medicus
Journal Article
Lancashire Evening Post (Preston, England), ISSN 0964-0967, 09/2019
Newspaper Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 09/2019, Volume 42, Issue 5, pp. 944 - 954
Mutations in at least 13 different genes (called CLN s) underlie various forms of neuronal ceroid lipofuscinoses (NCLs), a group of the most common... 
neurodegeneration | palmitoyl‐protein thioesterase‐1 | lysosomal storage disease | infantile neuronal ceroid lipofuscinosis | juvenile neuronal ceroid lipofuscinosis | batten disease | Index Medicus
Journal Article