SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies | Journal of Neurology, Neurosurgery & Psychiatry

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SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies

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Cite this article as:: Klein CJ, Wu Y, Kruckeberg KE, et al

SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies

Journal of Neurology, Neurosurgery & Psychiatry 2005;76:1022-1024.