Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy. [electronic resource]
Producer: 20020318Description: 151-8 p. digitalISSN:- 0960-8966
- Amino Acid Sequence
- Animals
- Biopsy
- DNA Primers
- Female
- Genetic Linkage
- Genetic Markers
- Haplotypes -- genetics
- Humans
- Male
- Molecular Sequence Data
- Muscle, Skeletal -- pathology
- Mutation
- Mutation, Missense
- Myopathies, Nemaline -- genetics
- Pedigree
- Polymorphism, Single-Stranded Conformational
- Protein Conformation
- Reverse Transcriptase Polymerase Chain Reaction
- Sequence Alignment
- Sequence Homology, Amino Acid
- Tropomyosin -- chemistry
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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