The phenotype of limb-girdle muscular dystrophy type 2I. [electronic resource]
Producer: 20040114Description: 1246-51 p. digitalISSN:- 1526-632X
- Adolescent
- Adult
- Amino Acid Substitution
- Child
- DNA Mutational Analysis
- Disease Progression
- Female
- Genotype
- Heart Failure -- etiology
- Humans
- Laminin -- deficiency
- Magnetic Resonance Imaging
- Male
- Middle Aged
- Muscle, Skeletal -- chemistry
- Muscular Dystrophies -- classification
- Mutation, Missense
- Pentosyltransferases
- Phenotype
- Point Mutation
- Proteins -- genetics
- Respiratory Insufficiency -- etiology
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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