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Full Description
This volume provides a contemporary evaluation of a diverse group of hereditary neuropathies. Its coverage of the application of the molecular genetic techniques of linkage and restriction fragment analysis to gene localization in disease focuses on the X chromosome and chromosome 1 as sites of CMT gene loci.
Contents
Clinical studies of CMT spanning decades and recording the incidence of pathological alterations in the populations of India and China; the clinical neurophysiologic assessment of pathophysiologic changes in peroneal muscular atrophy; axonal and Schwann metabolism and immune factors; the molecular genetic analysis of neuropathic disease, including linkage studies on peroneal muscular atrophies; metabolic studies of CMT syndromes and experimental drug trials with gangliosides, TRH and fatty acid supplementation.
