Phenotypic consequences of a novel SCO2 gene mutation

Medicine and Dentistry

• Muscle Biopsy 100%
• Hypertrophic Cardiomyopathy 100%
• Gene Mutation 100%
• Inborn Error of Metabolism 50%
• Neonatal Infant 50%
• Congestive Heart Failure 50%
• Diagnostic Testing 50%
• Pregnancy 50%
• Congenital Malformation 50%
• Genetic Screening 50%
• Skeletal Muscle 50%
• Myocardial Disease 50%
• Nonsense Mutation 50%
• Biochemical Analysis 50%
• Amniocentesis 50%
• Hypotonia 50%
• Oxidoreductase 50%
• Oxidative Phosphorylation 50%
• Cytochrome C Oxidase 50%