Linked Life Data

15842381

Source:http://linkedlifedata.com/resource/pubmed/id/15842381

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2005-4-21
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1538-7933
pubmed:author
pubmed:issnType
Print
pubmed:volume
3
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
808-11
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15842381-Child, pubmed-meshheading:15842381-Codon, pubmed-meshheading:15842381-DNA Primers, pubmed-meshheading:15842381-Exons, pubmed-meshheading:15842381-Factor IX, pubmed-meshheading:15842381-Factor XI, pubmed-meshheading:15842381-Factor XI Deficiency, pubmed-meshheading:15842381-Female, pubmed-meshheading:15842381-Genotype, pubmed-meshheading:15842381-Hemophilia B, pubmed-meshheading:15842381-Hemorrhage, pubmed-meshheading:15842381-Humans, pubmed-meshheading:15842381-Introns, pubmed-meshheading:15842381-Leucine, pubmed-meshheading:15842381-Male, pubmed-meshheading:15842381-Mutation, pubmed-meshheading:15842381-Mutation, Missense, pubmed-meshheading:15842381-Phenotype, pubmed-meshheading:15842381-Phenylalanine, pubmed-meshheading:15842381-Polymerase Chain Reaction, pubmed-meshheading:15842381-Serine, pubmed-meshheading:15842381-Tyrosine, pubmed-meshheading:15842381-Valine
pubmed:year
2005
pubmed:articleTitle
Novel missense mutations in two patients with factor XI deficiency (Val271Leu and Tyr351Ser) and one patient with combined factor XI and factor IX deficiency (Phe349Val).
pubmed:publicationType
Letter, Research Support, Non-U.S. Gov't