Creutzfeldt-Jakob disease in a young person with valine homozygosity at codon 129: sporadic or variant?
| Autor: | Hillier, C E, Llewelyn, J G, Neal, J W, Ironside, J W |
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| Zdroj: | Journal of Neurology, Neurosurgery & Psychiatry; Jan2001, p134-135, 2p |
| Databáze: | Complementary Index |
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