Hereditory Sensory Neuropathy Type 1 (SPTLC1): phenotypic variation in patients with the English founder mutation
Umaiyal Kugathasan(National Hospital for Neurology and Neurosurgery), Mary M. Reilly(National Hospital for Neurology and Neurosurgery), James M. Polke(National Hospital for Neurology and Neurosurgery), Rahul Phadke(MRC Prion Unit), David Bennett(University of Oxford), Thorsten Hornemann(University Hospital of Zurich), G. Lauria, Pedro José Tomaselli(Universidade de São Paulo), Saranya Suriyanarayanan(University Hospital Zurich), Henry Houlden(Queen Mary University of London), Caroline Sinclair, M.R.B. Evans, Raffaella Lombardi(Apple (Israel)), J. Blake, A. Pittmann
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