Charcot-Marie-Tooth Disorders
Pathophysiology, Molecular Genetics and Therapy
Seiten
1990
John Wiley & Sons Inc (Verlag)
978-0-471-56234-4 (ISBN)
John Wiley & Sons Inc (Verlag)
978-0-471-56234-4 (ISBN)
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A contemporary evaluation of a diverse group of hereditary neuropathies. It discusses the application of the molecular-genetic techniques of linkage and fragment analysis to gene localization in disease, focusing on the X chromosome and chromosome 1 as sites of CMT gene loci.
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.
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.
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.
| Reihe/Serie | Neurology & Neurobiology S. ; Vol 53 |
|---|---|
| Zusatzinfo | Ill. |
| Verlagsort | New York |
| Sprache | englisch |
| Maße | 155 x 235 mm |
| Gewicht | 1021 g |
| Themenwelt | Studium ► 2. Studienabschnitt (Klinik) ► Pathologie |
| Naturwissenschaften ► Biologie ► Genetik / Molekularbiologie | |
| ISBN-10 | 0-471-56234-3 / 0471562343 |
| ISBN-13 | 978-0-471-56234-4 / 9780471562344 |
| Zustand | Neuware |
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