DDX58 and Classic Singleton-Merten Syndrome

Medicine and Dentistry

• Syndrome 100%
• Phenotype 40%
• Interferon Type I 40%
• Dentinogenesis Imperfecta 40%
• Tendon Rupture 40%
• Association 20%
• Prognosis 20%
• Psoriasis 20%
• Cells 20%
• Blood 20%
• Mutant 20%
• Calcification 20%
• Arthropathy 20%
• Family 20%
• Inpatient 20%
• Glaucoma 20%
• Promoter Region 20%
• Polyinosinic Polycytidylic Acid 20%
• Autosomal Dominant Inheritance 20%
• Sequela 20%
• Upregulation 20%
• Skeleton Malformation 20%
• Gain of Function Mutation 20%
• Interferon Production 20%

Biochemistry, Genetics and Molecular Biology

• Next Generation Sequencing 40%
• Phenotype 40%
• Dysplasia 40%
• Interferon Type I 40%
• Mutation 20%
• Mutant 20%
• Association 20%
• Wild Type 20%
• Promoter Region 20%
• Autosomal Dominant Inheritance 20%
• Upregulation 20%
• Gain of Function Mutation 20%
• Interferon Production 20%