8401517

Source:http://linkedlifedata.com/resource/pubmed/id/8401517

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0020792, umls-concept:C0026882, umls-concept:C0029434, umls-concept:C0041455, umls-concept:C1332773, umls-concept:C1333079
pubmed:issue	8
pubmed:dateCreated	1993-11-5
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9208958
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Codon, http://linkedlifedata.com/resource/pubmed/chemical/Collagen, http://linkedlifedata.com/resource/pubmed/chemical/Glycine, http://linkedlifedata.com/resource/pubmed/chemical/Nucleic Acid Heteroduplexes, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Serine, http://linkedlifedata.com/resource/pubmed/chemical/Valine
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	0964-6906
pubmed:author	pubmed-author:GlorieuxF HFH, pubmed-author:RoughleyP JPJ, pubmed-author:SztrolovicsRR, pubmed-author:van der RestMM
pubmed:issnType	Print
pubmed:volume	2
pubmed:geneSymbol	COL1A2
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1319-21
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:8401517-Amino Acid Sequence, pubmed-meshheading:8401517-Base Sequence, pubmed-meshheading:8401517-Cell Line, pubmed-meshheading:8401517-Codon, pubmed-meshheading:8401517-Collagen, pubmed-meshheading:8401517-Female, pubmed-meshheading:8401517-Fibroblasts, pubmed-meshheading:8401517-Glycine, pubmed-meshheading:8401517-Humans, pubmed-meshheading:8401517-Infant, Newborn, pubmed-meshheading:8401517-Male, pubmed-meshheading:8401517-Molecular Sequence Data, pubmed-meshheading:8401517-Nucleic Acid Heteroduplexes, pubmed-meshheading:8401517-Osteogenesis Imperfecta, pubmed-meshheading:8401517-Point Mutation, pubmed-meshheading:8401517-RNA, Messenger, pubmed-meshheading:8401517-Serine, pubmed-meshheading:8401517-Skin, pubmed-meshheading:8401517-Valine
pubmed:year	1993
pubmed:articleTitle	Identification of type I collagen gene (COL1A2) mutations in nonlethal osteogenesis imperfecta.
pubmed:affiliation	Genetics Unit, Shriners Hospital for Crippled Children, Montreal, Quebec, Canada.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't