PN09 - Hereditory Sensory Neuropathy Type 1 (SPTLC1): phenotypic variation in patients with the English founder mutation

Saved in:
Bibliographic Details
Published inNeuromuscular disorders : NMD Vol. 27; pp. S26 - S27
Main Authors Kugathasan, U., Laurá, M., Tomaselli, P.J., Evans, M.R.B., Pittmann, A., Sinclair, C.J.D., Hornemann, T., Suriyanarayanan, S., Phadke, R., Lauria, G., Lombardi, R., Polke, J.M., Bennett, D.L., Houlden, H., Blake, J., Reilly, M.M.
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.03.2017
Online AccessGet full text

Cover

More Information
ISSN:0960-8966
1873-2364
DOI:10.1016/S0960-8966(17)30296-1