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- Lysosomale Sykdommer
- Downloaded from Pharmgkb (Accessed 11/2018 by Webgestalt 334 Tool)) Databases
- Gene and Disease List
- Identification of Two Novel Null Variants in CLN8 By
- Three Mutations That Cause Fifferent Forms of Canine Neuronal Ceroid Lipofuscinosis
- CLN8 Is an ER Cargo Receptor That Regulates Lysosome Biogenesis
- Cln3p Impacts Galactosylceramide Transport, Raft Morphology, and Lipid Content
- Comprehensive Lysosomal Storage Disorders Panel with GBA and IDS
- CLN8 Gene CLN8, Transmembrane ER and ERGIC Protein
- Neuronal Ceroid-Lipofuscinosis, CLN3-Related
- Mutation Leading to a Sulfatase Deficiency Is Associated
- Abnormal Sphingolipid World in Inflammation Specific for Lysosomal
- Targeted Genes and Methodology Details for Inborn Errors of Metabolism Custom Gene Panel
- Neuronal Ceroid Lipofuscinosis: a Common Pathway?
- Lysosomal Storage Disease Overview
- From Gene to Behavior: Investigation of Ppt1 and Ppt2 Rnai Induced Knock-Down During Drosophila Neurogenesis Patrick J
- Lysosomes As a Therapeutic Target
- 1 AAV9 Gene Therapy Restores Lifespan and Treats Pathological And
- A CLN8 Nonsense Mutation in the Whole Genome Sequence of a Mixed Breed Dog with Neuronal Ceroid Lipofuscinosis and Australian Shepherd Ancestry
- (CLN6) and in Nclf Mutant Mice Encodes a Novel Predicted Transmembrane Protein Ruth B
- Requisition for DNA Testing Reason for Referral: Sample Collection
- “Atypical” Phenotypes of Neuronal Ceroid Lipofuscinosis
- Horizontal Gene Transfer of an Entire Metabolic Pathway Between a Eukaryotic Alga and Its DNA Virus
- Horizontal Gene Transfer of an Entire Metabolic Pathway Between a Eukaryotic Alga and Its DNA Virus
- A CLN6-CLN8 Complex Recruits Lysosomal Enzymes at the ER for Golgi Transfer
- CLN8 Disease
- STAT Autism and Intellectual Disability Panel
- Supplementary Data
- Epilepsy Test Requisition
- Genomic Unity® Testing Comprehensive Neurology Testing Services Obtaining a Molecular Diagnosis for Neurology Patients Can Be Challenging
- A Mouse Model of Classical Late-Infantile Neuronal Ceroid Lipofuscinosis Based on Targeted Disruption of the CLN2 Gene Results I
- Neuronal Ceroid Lipofuscinoses Type 8: Expanding Genotype/ Phenotype Diversity-First Report from Saudi Arabia
- Genetix Panels Gene List FINAL
- CLN5, 6, 7 & 8) Adult Neuronal Ceroid-Lipofuscinosis (CLN6
- Natural History of JNCL and Other Ncls
- Emerging New Roles of the Lysosome and Neuronal Ceroid Lipofuscinoses Anil B
- Drosophila Responses in Immunity And
- Gene Therapy Rescues Pathological Deficits, Improves Behavioral Aspects, and Prolongs Survival in CLN3-, CLN6-, and CLN8-Batten Disease Jacob T
- Genomic Unity® Neurology Analysis