Clinical and genetic analysis of four Taiwanese families with autosomal dominant hereditary spastic paraplegia

Biochemistry, Genetics and Molecular Biology

• Genetics 100%
• Autosomal Dominant Inheritance 100%
• Nested Gene 75%
• Exon 75%
• Mutation 50%
• Protein Sequencing 50%
• Phenotype 25%
• Sequencing 25%
• Age 25%
• Gene Mutation 25%
• Missense Mutation 25%
• Multiplex Ligation-Dependent Probe Amplification 25%

Medicine and Dentistry

• Family 100%
• Genetic Analysis 100%
• Autosomal Dominant Inheritance 100%
• DeJerine-Sottas Disease 100%
• Gene 37%
• Exon 37%
• Sequence Analysis 25%
• Phenotype 12%
• Disease 12%
• Assessment 12%
• Patient 12%
• Clinical Feature 12%
• Missense Mutation 12%
• Onset Age 12%

Neuroscience

• Gene 37%
• Exon 37%
• Neurodegenerative Disorder 12%
• Phenotype 12%
• Missense Mutation 12%
• Multiplex Ligation-Dependent Probe Amplification 12%