A novel nemaline myopathy in the Amish caused by a mutation in troponin T1

Biochemistry, Genetics and Molecular Biology

• Troponin 100%
• TNNT1 100%
• Linkage Analysis 50%
• Autosomal Recessive Inheritance 50%
• Amino Acids 50%
• Skeletal Muscle 50%
• Exon 50%
• Pedigree 50%
• Protein Filament 50%
• Troponin T 50%
• Stop Codon 50%

Neuroscience

• Muscle Disorder 100%
• Troponin 100%
• Amino Acid 20%
• Tremor 20%
• Exon 20%
• Skeletal Muscle 20%
• Protein Filament 20%
• Troponin T 20%
• Hypotonia 20%
• Stop Codon 20%

Keyphrases

• Nemaline 20%