Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia

Keyphrases

• Common Haplotype 100%
• Autosomal Recessive Cerebellar Ataxia 100%
• Single nucleotide Polymorphism 50%
• Japan 50%
• Genetic mutation 50%
• Genomic Regions 50%
• Pathogenic mutations 50%
• Haplotype Analysis 50%
• Microsatellite Markers 50%
• Recombination Event 50%
• Online Mendelian Inheritance in Man 50%
• Cerebellar Ataxia 50%
• Founder Effect 50%

Biochemistry, Genetics and Molecular Biology

• Haplotype 100%
• Autosomal Dominant Inheritance 100%
• Single-Nucleotide Polymorphism 33%
• Mendelian Inheritance 33%
• Gene Mutation 33%
• Microsatellite Marker 33%
• Founder Effect 33%
• Genomics 33%

Neuroscience

• Ataxia 100%
• Haplotype 100%
• Gene Mutation 33%
• Single-Nucleotide Polymorphism 33%
• Microsatellite 33%