A novel mutation of myelin protein zero associated with an axonal form of Charcot-Marie-Tooth disease.

Name: A novel mutation of myelin protein zero associated with an axonal form of Charcot-Marie-Tooth disease.
Author: Santoro, L

A novel mutation of myelin protein zero associated with an axonal form of Charcot-Marie-Tooth disease. — المؤلف: Santoro, L — Journal of neurology, neurosurgery, and psychiatry 20040311

المؤلف: Santoro, L
النشر: Journal of neurology, neurosurgery, and psychiatry 20040311
الوصف: 262-5 p.
الموضوعات: Aged؛ Axons؛ Charcot-Marie-Tooth Disease؛ Chromosomes, Human, Pair 17؛ Codon؛ DNA Mutational Analysis؛ Dipeptides؛ Electromyography