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The FEBS journal, ISSN 1742-464X, 02/2016, Volume 283, Issue 3, pp. 459 - 471
...‐derived neurotrophic factor CSF cerebrospinal fluid FABP fatty acid binding protein HMW high molecular weight INCL infantile neuronal ceroid lipofuscinosis JNCL... 
immunoassays | plasma biomarkers | 2D‐DIGE | NCL | 2D-DIGE | Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Blood Proteins - analysis | Immunoassay | Biomarkers - blood | Neuronal Ceroid-Lipofuscinoses - blood | Humans | Proteomics | Proteins | Biological markers | Neurons | Biomarkers | Index Medicus | Plasma Biomarkers | Immunoassays
Journal Article
Acta neuropathologica, ISSN 1432-0533, 12/2015, Volume 131, Issue 4, pp. 621 - 637
Journal Article
Documenta ophthalmologica, ISSN 1573-2622, 11/2018, Volume 138, Issue 1, pp. 55 - 70
Mutation of the CLN3 gene, associated with juvenile neuronal ceroid lipofuscinosis, has recently been associated with late-onset, non-syndromic retinal dystrophy... 
CLN3 | Autoimmune retinopathy | Medicine & Public Health | Splicing | Retinitis pigmentosa | Juvenile neuronal ceroid lipofuscinosis | Retina | Ophthalmology | Life Sciences & Biomedicine | Science & Technology | Exons | Autoantibodies - blood | Humans | Middle Aged | Neuronal Ceroid-Lipofuscinoses - physiopathology | Retina - immunology | Mutation, Missense | Neuronal Ceroid-Lipofuscinoses - immunology | Multimodal Imaging | Neuronal Ceroid-Lipofuscinoses - genetics | Retinal Dystrophies - immunology | Female | Retrospective Studies | Neuronal Ceroid-Lipofuscinoses - diagnosis | Visual Acuity - physiology | Electroretinography | Retina - physiopathology | Molecular Chaperones - genetics | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Retinal Dystrophies - physiopathology | Membrane Glycoproteins - genetics | Retinal Dystrophies - diagnosis | Pedigree | Autoantigens - immunology | Retinal Dystrophies - genetics | Case studies | Viral antibodies | Neurons | Antibodies | Genetic research | Retinal degeneration | DNA polymerases | Genetic aspects | Nucleotide sequencing | Genetic screening | DNA sequencing | Neuroimaging | RNA-directed DNA polymerase | Rituximab | Leukocytes | Gene deletion | Acuity | Electroretinograms | Polymerase chain reaction | CLN3 protein | Missense mutation | Immunology | Degeneration | Neuronal ceroid lipofuscinosis | Mutation | Index Medicus
Journal Article
Scientific reports, ISSN 2045-2322, 07/2019, Volume 9, Issue 1, pp. 9891 - 8
Journal Article
Scientific reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 6332 - 15
Mutations in the co-chaperone protein, CSP alpha, cause an autosomal dominant, adult-neuronal ceroid lipofuscinosis (AD-ANCL... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Presynapse | Axons | Lysosomal enzymes | Fibroblasts | Phagosomes | Lysosomes | Skin | Neuronal ceroid lipofuscinosis | Mutation | Exocytosis | Drug screening | Phagocytosis | Index Medicus
Journal Article
Journal of neurochemistry, ISSN 0022-3042, 05/2017, Volume 141, Issue 3, pp. 423 - 435
Journal Article
Human mutation, ISSN 1098-1004, 07/2019, Volume 40, Issue 11, pp. 1924 - 1938
Journal Article