A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies.
Muglia, Maria
A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies. [electronic resource] - Journal of the neurological sciences Dec 2007 - 194-7 p. digital
Publication Type: Journal Article
0022-510X
10.1016/j.jns.2007.05.034 doi
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
A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies. [electronic resource] - Journal of the neurological sciences Dec 2007 - 194-7 p. digital
Publication Type: Journal Article
0022-510X
10.1016/j.jns.2007.05.034 doi
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