DMD exon 1 truncating point mutations: Amelioration of phenotype by alternative translation initiation in exon 6

Keyphrases

• Point mutation 100%
• Exon 1 100%
• Exon 6 100%
• Duchenne muscular Dystrophy 100%
• Alternative Translation Initiation 100%
• Truncation Point 100%
• Exon 33%
• Dystrophin 33%
• Becker muscular Dystrophy 33%
• Molecular Mechanism 16%
• Disease Severity 16%
• Amino Acids 16%
• Severe Disease 16%
• N-terminus 16%
• Ambulation 16%
• Clinical Phenotype 16%
• Codon 16%
• Nonsense mutation 16%
• Progressive Weakness 16%
• First Exons 16%
• Translational Initiation 16%
• Translation Initiation 16%
• General Mechanism 16%
• Initiation Codon 16%
• Phenotypic Rescue 16%

Biochemistry, Genetics and Molecular Biology

• Point Mutation 100%
• Exon 100%
• Translation Initiation 100%
• Codon 33%
• Dystrophin 33%
• Amino Acids 16%
• N-Terminus 16%
• Isoform 16%
• Nonsense Mutation 16%