MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathy. [electronic resource]
Producer: 20070710Description: 321-9 p. digitalISSN:- 0960-8966
- Adult
- Aged
- Arginine -- genetics
- Cardiac Myosins -- genetics
- Child
- Family Health
- Female
- Humans
- Infant
- Magnetic Resonance Imaging
- Male
- Microscopy, Electron, Transmission
- Middle Aged
- Muscle, Skeletal -- pathology
- Muscular Diseases -- classification
- Muscular Dystrophy, Emery-Dreifuss -- genetics
- Mutation
- Myosin Heavy Chains -- genetics
- Myosins -- metabolism
- RNA, Messenger -- metabolism
- Reverse Transcriptase Polymerase Chain Reaction -- methods
- Tryptophan -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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