Pub. Date : 2016 Jan
PMID : 25851836
1 Functional Relationships(s)Download |
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Sentence | Compound Name | Protein Name | Organism |
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| 1 | The genotype (methionine, M or valine, V) at polymorphic codon 129 of the PRNP gene and the type (1 or 2) of abnormal prion protein in the brain are the major determinants of the clinicopathological features of sporadic Creutzfeldt-Jakob disease (CJD), thus providing molecular basis for classification of sporadic CJD, that is, MM1, MM2, MV1, MV2, VV1 or VV2. | Methionine | plexin B2 | Homo sapiens | ||