## Abstract The heterozygous TremblerβJ (TrJ/+) mouse, containing a point mutation in the peripheral myelin protein 22 (__Pmp22__) gene, is characterized by severe hypomyelination and is a representative model of CharcotβMarieβTooth 1A (CMT1A) disease/DejerineβSottas syndrome (DSS). Given that the
Animal models of peripheral neuropathy: The trembler mouse
β Scribed by J. G. McLeod; P. A. Low
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 958 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0148-639X
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β¦ Synopsis
Abstract
One of the features of the IVth International Congress on Neuromuscular Diseases, held in Montreal September 17β21, 1978, was a series of invited posters. In order to achieve a wider audience for this valuable material, we have made arrangements to publish a number of these posters in Muscle & Nerve. This is the third poster in this series. To preserve the original effect of the posters, they are being reproduced almost exactly as they appeared at the Congress, without editing or other alterations. We hope you will find this feature a useful addition to your Journal.
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