A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3

Keyphrases

• Copy number Variation 100%
• Autism 100%
• Becker muscular Dystrophy 100%
• Duchenne 100%
• TRPM3 100%
• Muscular Dystrophy 50%
• Genome Project 50%
• Exon 25%
• Comorbidity 25%
• Quantitative PCR 25%
• Duplication 25%
• Autism Spectrum Disorder 25%
• Late-onset 25%
• Ethical Issues 25%
• Fluorescence in Situ Hybridization 25%
• In Tandem 25%
• Exon 1 25%
• Genomic Characterization 25%
• Unexpected Findings 25%
• SNP Array 25%
• Genetic Etiology 25%
• Neurodevelopmental Disorders 25%
• PCR Amplification 25%
• Mild Symptoms 25%
• Multiplex Autism 25%
• Tandem Duplication 25%
• PCR-sequencing 25%
• Long-range PCR 25%
• Phenotypic Characterization 25%
• Genic 25%
• Multi-hit 25%
• DMD Gene 25%
• Junction Fragment 25%
• Genomic Background 25%
• Reading Frame Rule 25%

Biochemistry, Genetics and Molecular Biology

• Exon 100%
• TRPM3 100%
• Genetics 50%
• Single-Nucleotide Polymorphism 50%
• Real-Time Polymerase Chain Reaction 50%
• Fluorescence in Situ Hybridization 50%
• Genetic Background 50%
• Reading Frame 50%
• Genomics 50%
• Comorbidity 50%

Neuroscience

• Muscular Dystrophy 100%
• TRPM3 100%
• Autism 100%
• Exon 40%
• Genome Project 40%
• In Situ Hybridization 20%
• Real-Time Polymerase Chain Reaction 20%
• Single-Nucleotide Polymorphism 20%
• Pervasive Developmental Disorder 20%
• Neurodevelopmental Disorder 20%
• Reading Frame 20%
• Comorbidity 20%