Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. [electronic resource]
Producer: 20110411Description: 608-17 p. digitalISSN:- 1460-2156
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Arthrogryposis -- genetics
- Charcot-Marie-Tooth Disease -- genetics
- Child
- Female
- Hereditary Central Nervous System Demyelinating Diseases -- genetics
- Hereditary Sensory and Motor Neuropathy -- genetics
- Humans
- Male
- Middle Aged
- Mutation
- Myelin Proteins -- genetics
- Phenotype
- Sural Nerve -- pathology
- Transcription, Genetic
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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