Neuronal ceroid lipofuscinoses caused by defects in soluble lysosomal enzymes (CLN1 and CLN2)

Keyphrases

• Lysosomal Storage Disease 100%
• Neuronal Ceroid Lipofuscinosis 100%
• Lysosomal Enzymes 100%
• CLN1 100%
• CLN2 100%
• Juvenile Neuronal Ceroid Lipofuscinosis 100%
• Lysosomal Acid Lipase 66%
• Fatty Acids 33%
• Late-onset 33%
• Free Amino Acids 33%
• Molecular Genetics 33%
• Amino Acids 33%
• Biochemical Analysis 33%
• Storage Materials 33%
• Biochemical Genetics 33%
• Cysteine Residues 33%
• Amino-terminus 33%
• Clinical Genetics 33%
• Aminopeptidase I 33%
• Genetic Aspects 33%
• Protein-peptide Complex 33%
• Lipidated Proteins 33%
• Small Proteins 33%
• Palmitoyl-protein Thioesterase 1 33%
• Heterogeneous Nature 33%

Biochemistry, Genetics and Molecular Biology

• Enzyme 100%
• Batten Disease 100%
• Infantile Neuronal Ceroid Lipofuscinosis 100%
• Deficiency 100%
• Enzymatic Hydrolysis 33%
• Amino Acids 33%
• Molecular Genetics 33%
• Lipid 33%
• N-Terminus 33%
• Hydrolase 33%
• Peptidase 33%
• Palmitoyl Protein Thioesterase 33%
• Aminopeptidase I 33%
• Cysteine 33%
• Peptide 33%

Pharmacology, Toxicology and Pharmaceutical Science

• Lipofuscinosis 100%
• Lysosome Enzyme 100%
• Lysosome Storage Disease 75%
• Storage Disease 75%
• Fatty Acid 25%
• Amino Acid 25%
• Peptidase 25%
• Hydrolase 25%
• Enzymes 25%
• Cysteine 25%
• Lipid 25%
• Aminopeptidase I 25%
• Palmitoyl Protein Thioesterase 25%
• Peptide 25%