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Inherited neuropathies: new genes don't fit old models
1Department of Neurology, 464 Stemmler Hall, University of Pennsylvania School of Medicine, Philadelphia, 19104, USA.
Abstract:
Mutations in GARS cause dominantly inherited neuropathies in humans. GARS encodes glycyl-tRNA synthetase, the enzyme that couples glycine to its tRNA. In this issue of Neuron, Seburn et al. have identified and characterized a mutant mouse with a dominantly inherited axonal neuropathy caused by a Gars mutation that is inferred to have a gain of function.
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