9818868

Source:http://linkedlifedata.com/resource/pubmed/id/9818868

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017431, umls-concept:C0206042, umls-concept:C1853719
pubmed:issue	5
pubmed:dateCreated	1998-12-3
pubmed:abstractText	To report the clinical and pathologic features of patients with the D178N-129M mutation living in Germany.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Prions
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0028-3878
pubmed:author	pubmed-author:BodemerMM, pubmed-author:GieseAA, pubmed-author:KretzschmarH AHA, pubmed-author:KroppSS, pubmed-author:PoserSS, pubmed-author:RiedemannCC, pubmed-author:Schulz-SchaefferWW, pubmed-author:SkworcKK, pubmed-author:WindlOO, pubmed-author:ZerrII
pubmed:issnType	Print
pubmed:volume	51
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1398-405
pubmed:dateRevised	2008-11-21
pubmed:meshHeading	pubmed-meshheading:9818868-Adult, pubmed-meshheading:9818868-Aged, pubmed-meshheading:9818868-Amino Acid Substitution, pubmed-meshheading:9818868-Creutzfeldt-Jakob Syndrome, pubmed-meshheading:9818868-Female, pubmed-meshheading:9818868-Genetic Variation, pubmed-meshheading:9818868-Genotype, pubmed-meshheading:9818868-Germany, pubmed-meshheading:9818868-Humans, pubmed-meshheading:9818868-Male, pubmed-meshheading:9818868-Middle Aged, pubmed-meshheading:9818868-Phenotype, pubmed-meshheading:9818868-Prion Diseases, pubmed-meshheading:9818868-Prions, pubmed-meshheading:9818868-Restriction Mapping
pubmed:year	1998
pubmed:articleTitle	Phenotypic variability in fatal familial insomnia (D178N-129M) genotype.
pubmed:affiliation	Neurologische Klinik, Georg-August-Universität Göttingen, Germany.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't