Identification of a novel splicing mutation within SLC17A8 in a Korean family with hearing loss by whole-exome sequencing

Biochemistry, Genetics and Molecular Biology

• Next Generation Sequencing 100%
• Exome Sequencing 100%
• Autosomal Dominant Inheritance 100%
• Genotyping 50%
• Human 50%
• Linkage Analysis 50%
• Genetic Determinism 50%
• Sanger Sequencing 50%
• Mendelian Inheritance 50%

Immunology and Microbiology

• Next Generation Sequencing 100%
• Whole Exome Sequencing 100%
• Human 50%
• Sanger Sequencing 50%
• Heredity 50%