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P46 Clinical and genetic characterisation of hereditary sensory neuropathy type 1 caused by mutations in SPTLC2

✍ Scribed by S.M. Murphy; M. Laurá; D. Ernst; Y.-T. Liu; J. Blake; M. Donaghy; J. Winer; H. Houlden; T. Hornemann; M.M. Reilly

Book ID: 117670471
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 50 KB
Volume: 22
Category: Article
ISSN: 0960-8966
DOI: 10.1016/s0960-8966(12)70054-8

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