Analysis of spinocerebellar ataxia type 2 in Gunma Prefecture in Japan: CAG trinucleotide expansion and clinical characteristics

Medicine and Dentistry

• Spinocerebellar Ataxia 100%
• Patient 66%
• Allele 50%
• CAG Repeat 50%
• Onset Age 16%
• Autosomal Dominant Inheritance 16%
• Saccadic Eye Movement 16%
• Polyacrylamide Gel Electrophoresis 16%
• Spinocerebellar Ataxia Type 6 16%
• Anticipation 16%
• Hypotonia 16%
• Mosaicism 16%
• Hyporeflexia 16%
• Dentatorubral-Pallidoluysian Atrophy 16%
• Trinucleotide 16%
• Machado-Joseph Disease 16%
• Cells 16%
• Analysis 16%
• Female 16%
• Family 16%
• Tremor 16%
• Molecular Property 16%

Neuroscience

• Spinocerebellar Ataxia 100%
• CAG Repeat 50%
• Saccade 16%
• Polyacrylamide Gel Electrophoresis 16%
• Mosaicism 16%
• Hypotonia 16%
• Hyporeflexia 16%
• Spinocerebellar Ataxia Type-6 16%
• Trinucleotide 16%
• Tremor 16%

Biochemistry, Genetics and Molecular Biology

• Allele 50%
• CAG Repeat 50%
• Anticipation 16%
• Polyacrylamide Gel Electrophoresis 16%
• Spinocerebellar Ataxia Type 6 16%
• Age 16%
• Autosomal Dominant Inheritance 16%
• Saccadic Eye Movement 16%
• Mosaicism 16%
• Machado-Joseph Disease 16%