Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
1999-6-30
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1059-7794
pubmed:author
pubmed:issnType
Print
pubmed:volume
Suppl 1
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
S125-7
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:9452063-Achondroplasia, pubmed-meshheading:9452063-Amino Acid Sequence, pubmed-meshheading:9452063-Amino Acid Substitution, pubmed-meshheading:9452063-Aspartic Acid, pubmed-meshheading:9452063-Base Sequence, pubmed-meshheading:9452063-Calmodulin, pubmed-meshheading:9452063-Conserved Sequence, pubmed-meshheading:9452063-DNA, Complementary, pubmed-meshheading:9452063-DNA Mutational Analysis, pubmed-meshheading:9452063-Extracellular Matrix Proteins, pubmed-meshheading:9452063-Glycine, pubmed-meshheading:9452063-Glycoproteins, pubmed-meshheading:9452063-Humans, pubmed-meshheading:9452063-Male, pubmed-meshheading:9452063-Middle Aged, pubmed-meshheading:9452063-Molecular Sequence Data, pubmed-meshheading:9452063-Point Mutation, pubmed-meshheading:9452063-Repetitive Sequences, Nucleic Acid
pubmed:year
1998
pubmed:articleTitle
Pseudoachondroplasia due to the substitution of the highly conserved Asp482 by Gly in the seventh calmodulin-like repeat of cartilage oligomeric matrix protein.
pubmed:affiliation
Centre for the Study of Heritable Connective Tissue Diseases, Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada.
pubmed:publicationType
Journal Article, Case Reports, Research Support, Non-U.S. Gov't