Á lódáil...
Creutzfeldt-Jakob disease in a young person with valine homozygosity at codon 129: sporadic or variant?
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| Main Authors: | , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
BMJ Group
2001
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1763448/ https://ncbi.nlm.nih.gov/pubmed/11118269 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.70.1.134 |
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