Genetic analysis of SS18L1 in French amyotrophic lateral sclerosis

Biochemistry, Genetics and Molecular Biology

• Genetics 100%
• Exon 100%
• Amino Acids 50%
• Intron 50%
• Single-Nucleotide Polymorphism 50%
• Exome Sequencing 50%
• Motor Neuron 50%
• Chromatin Remodeling 50%
• Missense Mutation 50%

Neuroscience

• Amyotrophic Lateral Sclerosis 100%
• Exon 22%
• Amino Acid 11%
• Chromatin Assembly and Disassembly 11%
• Missense Mutation 11%
• Exome Sequencing 11%
• Motor Neuron Disease 11%
• Single-Nucleotide Polymorphism 11%
• Intron 11%