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- W2149151488 endingPage "1314" @default.
- W2149151488 startingPage "1304" @default.
- W2149151488 abstract "The genetic neuropathies are a clinically and genetically heterogeneous group of diseases of which the most common types are Charcot–Marie–Tooth disease (CMT), the hereditary sensory and autonomic neuropathies and the distal hereditary motor neuropathies. More than 30 causative genes have been described, making an accurate genetic diagnosis increasingly possible. Although no specific therapies are yet available, research into their pathogenesis has revolutionised our understanding of the peripheral nervous system and allowed the development of rational approaches to therapy. The first therapeutic trials in CMT are currently underway. This review will suggest an approach to the diagnosis of these disorders and provide an update on new therapies." @default.
- W2149151488 created "2016-06-24" @default.
- W2149151488 creator A5021057974 @default.
- W2149151488 creator A5024191252 @default.
- W2149151488 date "2009-11-16" @default.
- W2149151488 modified "2023-10-10" @default.
- W2149151488 title "Diagnosis and new treatments in genetic neuropathies" @default.
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