Linked Life Data

7757089

Source:http://linkedlifedata.com/resource/pubmed/id/7757089

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1995-6-29
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0964-6906
pubmed:author
pubmed:issnType
Print
pubmed:volume
4
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
319-20
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:7757089-Adolescent, pubmed-meshheading:7757089-Amino Acid Metabolism, Inborn Errors, pubmed-meshheading:7757089-Amino Acid Sequence, pubmed-meshheading:7757089-Base Sequence, pubmed-meshheading:7757089-Blotting, Western, pubmed-meshheading:7757089-Canada, pubmed-meshheading:7757089-DNA, pubmed-meshheading:7757089-Exons, pubmed-meshheading:7757089-Female, pubmed-meshheading:7757089-Humans, pubmed-meshheading:7757089-Hydrolases, pubmed-meshheading:7757089-Infant, Newborn, pubmed-meshheading:7757089-Liver, pubmed-meshheading:7757089-Male, pubmed-meshheading:7757089-Molecular Sequence Data, pubmed-meshheading:7757089-Mutation, pubmed-meshheading:7757089-Norway, pubmed-meshheading:7757089-Peptides, pubmed-meshheading:7757089-Polymerase Chain Reaction, pubmed-meshheading:7757089-Sequence Analysis, DNA, pubmed-meshheading:7757089-Tyrosine
pubmed:year
1995
pubmed:articleTitle
Two novel mutations involved in hereditary tyrosinemia type I.
pubmed:affiliation
Laboratoire de Génétique Cellulaire et Développementale, Université Laval, Ste-Foy, Québec, Canada.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't