Peripheral myelin protein 22: Facts and
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Dr. Ueli Suter; G. J. Snipes
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Article
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1995
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John Wiley and Sons
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English
⚖ 751 KB
Mutations affecting the peripheral myelin protein 22 (PMP22) gene are associated with inherited motor and sensory neuropathies in mouse (Trembler and Trembler-J) and human (Charcot-Marie-Tooth disease type 1A and Dejerine-Sottas syndrome). Although genetic studies have established a critical role of