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 journalArticlepeer-review

32 Scopus citations
Original languageEnglish (US)
Pages (from-to)10-17
Number of pages8
Issue number1
StatePublished - Jan 1966

ASJC Scopus subject areas

  • Clinical Neurology

Cite this