1290170

Source:http://linkedlifedata.com/resource/pubmed/id/1290170

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011155, umls-concept:C0015127, umls-concept:C0015295, umls-concept:C0020792, umls-concept:C0033621, umls-concept:C0178499, umls-concept:C0332307, umls-concept:C1314792, umls-concept:C1413745, umls-concept:C1442161
pubmed:issue	4-5
pubmed:dateCreated	1993-3-22
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0326377
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Protein C
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0049-3848
pubmed:author	pubmed-author:ArakawaMM, pubmed-author:KoideTT, pubmed-author:SatoHH, pubmed-author:TawarayaHH, pubmed-author:TokunagaFF, pubmed-author:WakabayashiSS
pubmed:issnType	Print
pubmed:day	1
pubmed:volume	68
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	417-23
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:1290170-Amino Acid Sequence, pubmed-meshheading:1290170-Base Sequence, pubmed-meshheading:1290170-Blood Coagulation Disorders, pubmed-meshheading:1290170-Exons, pubmed-meshheading:1290170-Frameshift Mutation, pubmed-meshheading:1290170-Gene Deletion, pubmed-meshheading:1290170-Humans, pubmed-meshheading:1290170-Molecular Sequence Data, pubmed-meshheading:1290170-Pedigree, pubmed-meshheading:1290170-Protein C, pubmed-meshheading:1290170-Protein C Deficiency, pubmed-meshheading:1290170-Sequence Alignment
pubmed:year	1992
pubmed:articleTitle	Identification of one base deletion in exon IX of the protein C gene that causes a type I deficiency.
pubmed:affiliation	Department of Life Science, Faculty of Science, Himeji Institute of Technology, Hyogo, Japan.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't