UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

TRPV4 mutations and functional characterisation in a cohort of patients with hereditary neuropathy

Fawcett, K; Murphy, SM; Polke, J; Reilly, MM; Houlden, H; (2011) TRPV4 mutations and functional characterisation in a cohort of patients with hereditary neuropathy. In: NEUROMUSCULAR DISORDERS. (pp. S16 - S16). PERGAMON-ELSEVIER SCIENCE LTD

Full text not available from this repository.
Type: Proceedings paper
Title: TRPV4 mutations and functional characterisation in a cohort of patients with hereditary neuropathy
Event: United Kingdom Neuromuscular Translational Research Conference 2011
Location: London, ENGLAND
Dates: 2011-03-29 - 2011-03-30
URI: http://discovery.ucl.ac.uk/id/eprint/1305598
Downloads since deposit
0Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item