Spinocerebellar ataxia 28: A novel AFG3L2 mutation in a German family with young onset, slow progression and saccadic slowing

Neuroscience

• Spinocerebellar Ataxia 100%
• Gene Mutation 100%
• Adenosine Triphosphatase 100%
• Exon 50%
• Ataxia 33%
• Pyramidal Tract 33%
• Missense Mutation 33%
• Saccade 16%
• Proteinase 16%
• Purkinje Cell 16%
• KCNC3 16%
• Fibroblast Growth Factor 14 16%
• Dideoxynucleotide Sequencing 16%
• Amino Acid 16%
• PRKCG 16%

Biochemistry, Genetics and Molecular Biology

• Gene Mutation 100%
• ATPase 100%
• Exon 50%
• Missense Mutation 33%
• C-Terminus 16%
• Dideoxynucleotide Sequencing 16%
• Genetic Screening 16%
• Coding Region 16%
• Protease 16%
• Protein Catabolism 16%
• Amino Acid 16%
• TTBK2 16%
• PRKCG 16%
• FGF14 16%
• Purkinje Cell 16%