Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
1995-1-5
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0964-6906
pubmed:author
pubmed:issnType
Print
pubmed:volume
3
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1175-7
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:7981691-Amino Acid Sequence, pubmed-meshheading:7981691-Animals, pubmed-meshheading:7981691-Base Sequence, pubmed-meshheading:7981691-Blood Coagulation Disorders, pubmed-meshheading:7981691-Cattle, pubmed-meshheading:7981691-Chromosomes, Human, Pair 13, pubmed-meshheading:7981691-DNA Mutational Analysis, pubmed-meshheading:7981691-Factor VII, pubmed-meshheading:7981691-Factor X, pubmed-meshheading:7981691-Female, pubmed-meshheading:7981691-Genes, pubmed-meshheading:7981691-Humans, pubmed-meshheading:7981691-Male, pubmed-meshheading:7981691-Molecular Sequence Data, pubmed-meshheading:7981691-Pedigree, pubmed-meshheading:7981691-Point Mutation, pubmed-meshheading:7981691-Polymerase Chain Reaction, pubmed-meshheading:7981691-Sequence Alignment, pubmed-meshheading:7981691-Sequence Homology, Amino Acid
pubmed:year
1994
pubmed:articleTitle
Topologically equivalent mutations causing dysfunctional coagulation factors VII (294Ala-->Val) and X (334Ser-->Pro).
pubmed:affiliation
Centro Studi Biochimici Patologie Genoma Umano-Dipartimento Biochimica e Biologia Molecolare, Università di Ferrara.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't