7849725

Source:http://linkedlifedata.com/resource/pubmed/id/7849725

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019904, umls-concept:C0030705, umls-concept:C0079301, umls-concept:C0205314, umls-concept:C0544885, umls-concept:C0679622, umls-concept:C1416786
pubmed:issue	10
pubmed:dateCreated	1995-3-16
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/P01-AR38923
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9208958
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers, http://linkedlifedata.com/resource/pubmed/chemical/Laminin
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0964-6906
pubmed:author	pubmed-author:BaudoinCC, pubmed-author:ChristianoA MAM, pubmed-author:Gagnoux-PalaciosLL, pubmed-author:MeneguzziGG, pubmed-author:MiquelCC, pubmed-author:OrtonneJ PJP, pubmed-author:PulkkinenLL, pubmed-author:TadiniGG, pubmed-author:UittoJJ
pubmed:issnType	Print
pubmed:volume	3
pubmed:geneSymbol	LAMC2
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1909-10
pubmed:dateRevised	2007-11-14
pubmed:meshHeading	pubmed-meshheading:7849725-Abortion, Induced, pubmed-meshheading:7849725-Base Sequence, pubmed-meshheading:7849725-Biopsy, pubmed-meshheading:7849725-Consanguinity, pubmed-meshheading:7849725-DNA Primers, pubmed-meshheading:7849725-Epidermolysis Bullosa, Junctional, pubmed-meshheading:7849725-Exons, pubmed-meshheading:7849725-Female, pubmed-meshheading:7849725-Fetus, pubmed-meshheading:7849725-Homozygote, pubmed-meshheading:7849725-Humans, pubmed-meshheading:7849725-Infant, pubmed-meshheading:7849725-Introns, pubmed-meshheading:7849725-Laminin, pubmed-meshheading:7849725-Male, pubmed-meshheading:7849725-Molecular Sequence Data, pubmed-meshheading:7849725-Open Reading Frames, pubmed-meshheading:7849725-Pedigree, pubmed-meshheading:7849725-Point Mutation, pubmed-meshheading:7849725-Polymerase Chain Reaction, pubmed-meshheading:7849725-Pregnancy, pubmed-meshheading:7849725-Skin
pubmed:year	1994
pubmed:articleTitle	A novel homozygous nonsense mutation in the LAMC2 gene in patients with the Herlitz junctional epidermolysis bullosa.
pubmed:affiliation	U385 INSERM, Faculté de Médecine, Nice, France.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Case Reports, Research Support, Non-U.S. Gov't