A single-base-pair deletion in the β-glucuronidase gene accounts for the phenotype of murine mucopolysaccharidosis type VII

Keyphrases

• Biochemical Abnormalities 25%
• Chromosome 5 25%
• Codon 25%
• DNA Fragments 25%
• DNA Sequence Analysis 25%
• DNA Sequencing 25%
• Enzyme Activity 25%
• Exon 10 50%
• Fibroblasts 25%
• Flanking Sequence 25%
• Fluorometric Assay 25%
• Frameshift mutation 50%
• Genomic DNA (gDNA) 25%
• Inherited Disease 25%
• Length Variation 25%
• Molecular Abnormalities 25%
• MRNA Level 25%
• Mucopolysaccharidosis VII 100%
• Mutated Genes 25%
• Non-denaturing 25%
• Oligonucleotides 25%
• Pathological Abnormalities 25%
• Polyacrylamide (PAAm) 25%
• Premature Stop Codon 25%
• Restriction Enzyme 25%
• Restriction Fragment Length 25%
• Restriction Sites 25%
• Sequencing Gel 25%
• Single Base 100%
• Site-directed mutagenesis 25%
• Spontaneous mutation 25%
• Structural Genes 25%
• β-glucuronidase 100%

Biochemistry, Genetics and Molecular Biology

• Allele 50%
• Beta-Glucuronidase 100%
• Chromosome 5 25%
• Codon 25%
• DNA Flanking Region 25%
• DNA Sequence 50%
• Enzyme Activity 25%
• Exon 50%
• Fibroblast 25%
• Frameshift Mutation 50%
• Genomic Fragment 25%
• Genomics 25%
• Heritable Disease 25%
• Messenger RNA 25%
• Oligonucleotide 25%
• Restriction Enzyme 25%
• Restriction Fragment 25%
• Restriction Site 25%
• Site-Directed Mutagenesis 25%
• Sly Syndrome 100%
• Spontaneous Mutation 25%
• Stop Codon 25%
• Structural Gene 25%