Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B [4]

J. M. Vance, M. C. Speer, J. M. Stajich, S. West, C. Wolpert, P. Gaskell, F. Lennon, R. M. Tim, M. Rozear, K. B. Othmane, M. A. Pericak-Vance, W. C. Yee, J. L. Elliott, J. M. Kwon, P. Goodfellow

Research output: Contribution to journalLetter

37 Scopus citations
Original languageEnglish (US)
Pages (from-to)258-262
Number of pages5
JournalAmerican journal of human genetics
Volume59
Issue number1
StatePublished - Jun 27 1996
Externally publishedYes

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Vance, J. M., Speer, M. C., Stajich, J. M., West, S., Wolpert, C., Gaskell, P., Lennon, F., Tim, R. M., Rozear, M., Othmane, K. B., Pericak-Vance, M. A., Yee, W. C., Elliott, J. L., Kwon, J. M., & Goodfellow, P. (1996). Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B [4]. American journal of human genetics, 59(1), 258-262.