Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single center

Keyphrases

• Single Center 100%
• Mutation Spectrum 100%
• Dystrophin Gene 100%
• Becker muscular Dystrophy 100%
• Consecutive Analysis 100%
• Duchenne 100%
• Duplication 66%
• Sequence Variation 66%
• Ethnic Groups 33%
• Genetic Characterization 33%
• Nerve 33%
• Small Variation 33%
• Duchenne muscular Dystrophy 33%
• Direct Sequencing 33%
• Nonsense mutation 33%
• Molecular Therapeutics 33%
• Multiplex Ligation-dependent Probe Amplification 33%
• Proband 33%
• Large Rearrangements 33%
• Muscle Disease 33%
• Therapeutic Trial 33%
• Registration System 33%
• X-linked Disorder 33%
• Dystrophin 33%
• Dystrophinopathy 33%
• Novel Variation 33%

Medicine and Dentistry

• Dystrophin 100%
• Becker Muscular Dystrophy 100%
• Ethnic Group 25%
• Combination Therapy 25%
• Duchenne Muscular Dystrophy 25%
• Nonsense Mutation 25%
• Multiplex Ligation Dependent Probe Amplification 25%
• Muscle Innervation 25%
• Muscle Disease 25%
• Dystrophinopathy 25%

Biochemistry, Genetics and Molecular Biology

• Dystrophin 100%
• Genetics 25%
• Nonsense Mutation 25%
• Multiplex Ligation-Dependent Probe Amplification 25%
• Proband 25%
• Muscle Innervation 25%