A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy. [electronic resource]
Producer: 20160719Description: e1005829 p. digitalISSN:- 1553-7404
- Amino Acid Sequence
- Animals
- Charcot-Marie-Tooth Disease -- genetics
- Chromosome Segregation
- Computer Simulation
- Demyelinating Diseases -- genetics
- Electrophysiological Phenomena
- Family
- Female
- Genes, Dominant
- HEK293 Cells
- Humans
- Leg -- physiopathology
- Magnetic Resonance Imaging
- Male
- Mice, Transgenic
- Molecular Sequence Data
- Mutation
- Myelin P2 Protein -- chemistry
- Pedigree
- Phenotype
- Sural Nerve -- pathology
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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