טוען...
Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob disease
BACKGROUND: Inherited prion diseases are rare autosomal dominant disorders associated with diverse clinical presentations. All are associated with mutation of the gene that encodes prion protein (PRNP). Homozygous mutations with atypical clinical phenotypes have been described but are extremely rare...
שמור ב:
| הוצא לאור ב: | BMC Neurol |
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| Main Authors: | , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2021
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8237416/ https://ncbi.nlm.nih.gov/pubmed/34182938 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-021-02274-w |
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