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SPTLC1 mutation in twin sisters with hereditary sensory neuropathy type I
Verhoeven, K., Coen, K., De Vriendt, E., Jacobs, A., Van Gerwen, V., Smouts, I., Pou-Serradell, A., Martin, J. -J., Timmerman, V., De Jonghe, P.Volume:
62
Language:
english
Journal:
Neurology
DOI:
10.1212/01.wnl.0000115388.10828.5c
Date:
March, 2004
File:
PDF, 118 KB
english, 2004