Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: Exclusion of GNE and three other candidate genes

Keyphrases

• Clinical Heterogeneity 100%
• Genetic Heterogeneity 100%
• Mutation Analysis 100%
• Inclusion Body Myopathy 100%
• IBMPFD 100%
• Chromosome 9p 100%
• Hereditary Myopathy 100%
• IBM-2 100%
• Autosomal Dominant 50%
• Frontotemporal Dementia 50%
• Paget's Disease of Bone 50%
• Limb-girdle muscular Dystrophy 50%
• Expression Study 50%
• Tropomyosin 50%
• Splice Variant 50%
• SMU1 50%
• GNE Gene 50%
• Quadriceps Sparing 50%
• Critical Locus 50%
• NDUFB6 50%

Biochemistry, Genetics and Molecular Biology

• Candidate Gene 100%
• Genetic Heterogeneity 100%
• Chromosome 9p 100%
• Autosomal Dominant Inheritance 50%
• Tropomyosin 50%
• GNE (Gene) 50%

Neuroscience

• Muscle Disorder 100%
• Chromosome 9p 100%
• Frontotemporal Dementia 33%
• Muscular Dystrophy 33%
• Tropomyosin 33%