Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies

Biochemistry, Genetics and Molecular Biology

• Mutation 100%
• TPM2 70%
• Phenotype 30%
• Tropomyosin 30%
• Nested Gene 20%
• Skeletal Muscle 10%
• Isoform 10%
• Data Base 10%
• Computer Model 10%
• Actin 10%
• Autosomal Dominant Inheritance 10%
• Genotype Phenotype Correlation 10%
• Association 10%

Medicine and Dentistry

• Phenotype 30%
• Tropomyosin 30%
• Patient 30%
• Diseases 20%
• Contracture 20%
• Myopathy 20%
• Gene 20%
• Nemaline Myopathy 20%
• Actin 10%
• Autosomal Dominant Inheritance 10%
• Genotype Phenotype Correlation 10%
• Symptom 10%
• In Silico 10%
• Arthrogryposis 10%
• Skeletal Muscle 10%
• Association 10%
• Family 10%
• Joint 10%
• Syndrome 10%
• Jaw 10%
• Limb 10%