Different SPTLC1 mutations in hereditary sensory neuropathy type 1 are associated with distinct clinical phenotypes

P. J. Spring, J. M. Spies, J. L. Dawkins, D. Hulme, I. P. Blair, M. Kennerson, G. A. Nicholson

Research output: Contribution to journalMeeting abstractpeer-review

Original languageEnglish
Pages (from-to)84-84
Number of pages1
JournalJournal of the Peripheral Nervous System
Issue numbers1
Publication statusPublished - Jul 2007
Externally publishedYes
EventAnnual Meeting of the Peripheral Nerve Society - Snowbird
Duration: 14 Jul 200718 Jul 2007

Cite this