Comprehensive Mutation Analysis for Congenital Muscular Dystrophy: A Clinical PCR-Based Enrichment and Next-Generation Sequencing Panel

Medicine and Dentistry

• Next Generation Sequencing 100%
• Sanger Sequencing 80%
• Muscular Dystrophy 70%
• Diagnosis 50%
• Gene 40%
• Polymerase Chain Reaction 40%
• Muscle Disease 20%
• Diseases 10%
• Screening 10%
• Genotype 10%
• Exon 10%
• Development 10%
• Molecular Diagnosis 10%
• Analysis 10%
• Laboratory 10%
• Ethinylestradiol Plus Megestrol Acetate 10%
• Diagnostic Procedure 10%

Biochemistry, Genetics and Molecular Biology

• Mutation 40%
• Nested Gene 40%
• Genotyping 10%
• Exon 10%
• Screening 10%
• Development 10%
• Sample 10%