A mutation in the human ryanodine receptor gene associated with central core disease. [electronic resource]
Producer: 19931209Description: 46-50 p. digitalISSN:- 1061-4036
- Amino Acid Sequence
- Animals
- Base Sequence
- Calcium Channels -- genetics
- Chromosomes, Human, Pair 19
- Female
- Genes
- Genes, Dominant
- Humans
- Lod Score
- Male
- Malignant Hyperthermia -- genetics
- Molecular Sequence Data
- Muscle Proteins -- genetics
- Myopathies, Nemaline -- genetics
- Pedigree
- Point Mutation
- Polymerase Chain Reaction
- Rabbits
- Ryanodine Receptor Calcium Release Channel
- Sequence Alignment
- Sequence Homology, Amino Acid
- Species Specificity
- Swine
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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