| pubmed-article:2159587 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:2159587 | lifeskim:mentions | umls-concept:C0033164 | lld:lifeskim |
| pubmed-article:2159587 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:2159587 | lifeskim:mentions | umls-concept:C0751254 | lld:lifeskim |
| pubmed-article:2159587 | lifeskim:mentions | umls-concept:C0441587 | lld:lifeskim |
| pubmed-article:2159587 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:2159587 | pubmed:dateCreated | 1990-6-14 | lld:pubmed |
| pubmed-article:2159587 | pubmed:abstractText | In a pedigree with Creutzfeldt-Jakob disease we identified a 144-bp insertion in the open reading frame of the prion protein (PrP) gene. The insertion is in-frame and codes for 6 extra uninterrupted octapeptide repeats in addition to the 5 that are normally present in the N-terminal region of the protein. The possibility that this mutation may prove relevant to elucidating the mechanism of horizontal transmission of the spongiform encephalopathies is discussed. | lld:pubmed |
| pubmed-article:2159587 | pubmed:language | eng | lld:pubmed |
| pubmed-article:2159587 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2159587 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:2159587 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2159587 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2159587 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2159587 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:2159587 | pubmed:issn | 0169-328X | lld:pubmed |
| pubmed-article:2159587 | pubmed:author | pubmed-author:CrowT JTJ | lld:pubmed |
| pubmed-article:2159587 | pubmed:author | pubmed-author:BakerHH | lld:pubmed |
| pubmed-article:2159587 | pubmed:author | pubmed-author:OwenFF | lld:pubmed |
| pubmed-article:2159587 | pubmed:author | pubmed-author:PoulterMM | lld:pubmed |
| pubmed-article:2159587 | pubmed:author | pubmed-author:LofthouseRR | lld:pubmed |
| pubmed-article:2159587 | pubmed:author | pubmed-author:CollingeJJ | lld:pubmed |
| pubmed-article:2159587 | pubmed:author | pubmed-author:ShahTT | lld:pubmed |
| pubmed-article:2159587 | pubmed:author | pubmed-author:RidleyRR | lld:pubmed |
| pubmed-article:2159587 | pubmed:author | pubmed-author:McVeyJJ | lld:pubmed |
| pubmed-article:2159587 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2159587 | pubmed:volume | 7 | lld:pubmed |
| pubmed-article:2159587 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2159587 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2159587 | pubmed:pagination | 273-6 | lld:pubmed |
| pubmed-article:2159587 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:2159587 | pubmed:meshHeading | pubmed-meshheading:2159587-... | lld:pubmed |
| pubmed-article:2159587 | pubmed:meshHeading | pubmed-meshheading:2159587-... | lld:pubmed |
| pubmed-article:2159587 | pubmed:meshHeading | pubmed-meshheading:2159587-... | lld:pubmed |
| pubmed-article:2159587 | pubmed:meshHeading | pubmed-meshheading:2159587-... | lld:pubmed |
| pubmed-article:2159587 | pubmed:meshHeading | pubmed-meshheading:2159587-... | lld:pubmed |
| pubmed-article:2159587 | pubmed:meshHeading | pubmed-meshheading:2159587-... | lld:pubmed |
| pubmed-article:2159587 | pubmed:meshHeading | pubmed-meshheading:2159587-... | lld:pubmed |
| pubmed-article:2159587 | pubmed:year | 1990 | lld:pubmed |
| pubmed-article:2159587 | pubmed:articleTitle | An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease. | lld:pubmed |
| pubmed-article:2159587 | pubmed:affiliation | Division of Psychiatry, Clinical Research Centre, Harrow, Middlesex, U.K. | lld:pubmed |
| pubmed-article:2159587 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:2159587 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:5621 | entrezgene:pubmed | pubmed-article:2159587 | lld:entrezgene |
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