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Anatomy5

Liver Muscles Muscle, Skeletal Lysosomes Microsomes

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Dependovirus Mice, Knockout Dogs Adenoviridae

Diseases38

Glycogen Storage Disease Type I Glycogen Storage Disease Glycogen Storage Disease Type III Glycogen Storage Disease Type IV Glycogen Storage Disease Type II Glycogen Storage Disease Type VII Glycogen Storage Disease Type V Glycogen Storage Disease Type VI Lysosomal Storage Diseases Glycogen Storage Disease Type VIII Alzheimer Disease Adenoma, Liver Cell Enterocolitis Cholesterol Ester Storage Disease Hepatomegaly Metabolism, Inborn Errors Glycogen Storage Disease Type IIb Hypoglycemia Fructose-1,6-Diphosphatase Deficiency Lysosomal Storage Diseases, Nervous System Sialic Acid Storage Disease Wolman Disease alpha-Mannosidosis Sphingolipidoses Disease Models, Animal Dog Diseases Gaucher Disease Mucopolysaccharidosis VII Liver Neoplasms Lipid Metabolism, Inborn Errors Mucopolysaccharidosis I Lipidoses Neutropenia Adenoma Fucosidosis Carbohydrate Metabolism, Inborn Errors Aspartylglucosaminuria Sandhoff Disease

Chemicals and Drugs29

Glycogen Glucose-6-Phosphatase Glycogen Debranching Enzyme System alpha-Glucosidases Liver Glycogen Glycogen Synthase Glucan 1,4-alpha-Glucosidase Glucose-6-Phosphate Antiporters Amylopectin 1,4-alpha-Glucan Branching Enzyme Glycogen Phosphorylase Monosaccharide Transport Proteins Glycogen Synthase Kinase 3 Phosphorylase b Starch Phosphorylases Lactic Acid Glucose Lactates Hypoxanthine Uric Acid Blood Glucose Glycogen Synthase Kinases Inosine Hypoxanthines Insulin Purines Seed Storage Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

Drug Storage Drug Discovery Enzyme Replacement Therapy Genetic Therapy Disease Models, Animal Pedigree DNA Mutational Analysis Liver Transplantation Blood Preservation

Psychiatry and Psychology1

Alzheimer Disease

Phenomena and Processes9

Polymorphism, Single-Stranded Conformational Mutation Genetic Vectors Exons Heterozygote Base Sequence Point Mutation Mutation, Missense Amino Acid Sequence

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Technology, Industry, Agriculture1

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

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Glycogen Storage Disease Type I Glycogen Storage Disease Glycogen Storage Disease Type III Glycogen Storage Disease Type IV Glycogen Storage Disease Type II Drug Storage Glycogen Glycogen Storage Disease Type VII Glucose-6-Phosphatase Glycogen Storage Disease Type V Glycogen Debranching Enzyme System Drug Discovery Glycogen Storage Disease Type VI alpha-Glucosidases Lysosomal Storage Diseases Liver Glycogen Glycogen Synthase Glycogen Storage Disease Type VIII Alzheimer Disease Glucan 1,4-alpha-Glucosidase Glucose-6-Phosphate Antiporters Adenoma, Liver Cell Amylopectin 1,4-alpha-Glucan Branching Enzyme Enterocolitis Cholesterol Ester Storage Disease Hepatomegaly Glycogen Phosphorylase Metabolism, Inborn Errors Liver Enzyme Replacement Therapy Glycogen Storage Disease Type IIb Monosaccharide Transport Proteins Hypoglycemia Fructose-1,6-Diphosphatase Deficiency Glycogen Synthase Kinase 3 Phosphorylase b Starch Lysosomal Storage Diseases, Nervous System Phosphorylases Lactic Acid Sialic Acid Storage Disease Glucose Dependovirus Genetic Therapy Wolman Disease Muscles Lactates Muscle, Skeletal alpha-Mannosidosis Polymorphism, Single-Stranded Conformational Mutation Hypoxanthine Uric Acid Sphingolipidoses Blood Glucose Genetic Vectors Lysosomes Molecular Sequence Data Disease Models, Animal Glycogen Synthase Kinases Inosine Exons Mice, Knockout Hypoxanthines Dog Diseases Heterozygote Gaucher Disease Mucopolysaccharidosis VII Food Storage Base Sequence Liver Neoplasms Lipid Metabolism, Inborn Errors Pedigree Mucopolysaccharidosis I Point Mutation Mutation, Missense Dogs Amino Acid Sequence Lipidoses Neutropenia Microsomes Adenoma DNA Mutational Analysis Insulin Adenoviridae Purines Fucosidosis Seed Storage Proteins Carbohydrate Metabolism, Inborn Errors Aspartylglucosaminuria Sandhoff Disease Liver Transplantation Blood Preservation

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