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

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

Research output: Contribution to journalArticle

37 Citations (Scopus)
Original languageEnglish
Pages (from-to)258-262
Number of pages5
JournalAmerican Journal of Human Genetics
Volume59
Issue number1
StatePublished - Jun 27 1996
Externally publishedYes

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Hereditary Sensory and Autonomic Neuropathies
Lod Score
Charcot-Marie-Tooth Disease
Genetic Linkage
Chromosomes, Human, Pair 3
Type 2B Charcot-Marie-Tooth disease

ASJC Scopus subject areas

  • Genetics

Cite this

Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B [4]. / Vance, Jeffery 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, Margaret A; Yee, W. C.; Elliott, J. L.; Kwon, J. M.; Goodfellow, P.

In: American Journal of Human Genetics, Vol. 59, No. 1, 27.06.1996, p. 258-262.

Research output: Contribution to journalArticle

Vance, JM, Speer, MC, Stajich, JM, West, S, Wolpert, C, Gaskell, P, Lennon, F, Tim, RM, Rozear, M, Othmane, KB, Pericak-Vance, MA, Yee, WC, Elliott, JL, Kwon, JM & 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, vol. 59, no. 1, pp. 258-262.
Vance, Jeffery 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, Margaret A ; Yee, W. C. ; Elliott, J. L. ; Kwon, J. M. ; Goodfellow, P. / Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B [4]. In: American Journal of Human Genetics. 1996 ; Vol. 59, No. 1. pp. 258-262.
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