Quantitation of meissner’s corpuscles in hereditary neurologic disorders: Charcot-marie-tooth disease, roussy-levy syndrome, dejerine-sottas disease, hereditary sensory neuropathy, spinocerebellar degenerations, and hereditary spastic paraplegia

Peter J. Dyck, R. K. Winkelmann, Charles F. Bolton

Research output: Contribution to journal › Article › peer-review

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