A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies. [electronic resource]
Producer: 20080214Description: 194-7 p. digitalISSN:- 0022-510X
- Adolescent
- Chromosomes, Human, Pair 17
- DNA Mutational Analysis -- methods
- Exons -- genetics
- Family Health
- Female
- Hereditary Sensory and Motor Neuropathy -- complications
- Humans
- Italy
- Male
- Middle Aged
- Myelin Proteins -- genetics
- Neural Conduction -- physiology
- Paralysis -- complications
- Point Mutation
- Pressure
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Publication Type: Journal Article
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