Investigation for SPTLC1 mutations in a Taiwanese cohort with hereditary neuropathies

Autor: Hsiao, C.T., Chao, H.C., Liao, Y.C., Lin, K.P., Soong, B.W., Lee, Y.C.
Zdroj: In Journal of the Neurological Sciences 15 October 2017 381 Supplement:463-464
Databáze: ScienceDirect