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. |
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Zdroj: | In Journal of the Neurological Sciences 15 October 2017 381 Supplement:463-464 |
Databáze: | ScienceDirect |
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