12920092

Source:http://linkedlifedata.com/resource/pubmed/id/12920092

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Subject	Predicate	Object	Context
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pubmed-article:12920092	pubmed:issue	8	lld:pubmed
pubmed-article:12920092	pubmed:dateCreated	2003-8-15	lld:pubmed
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pubmed-article:12920092	pubmed:month	Aug	lld:pubmed
pubmed-article:12920092	pubmed:issn	1468-6244	lld:pubmed
pubmed-article:12920092	pubmed:author	pubmed-author:KENTA PAP	lld:pubmed
pubmed-article:12920092	pubmed:author	pubmed-author:CalzolariEE	lld:pubmed
pubmed-article:12920092	pubmed:author	pubmed-author:FerliniAA	lld:pubmed
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pubmed-article:12920092	pubmed:volume	40	lld:pubmed
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pubmed-article:12920092	pubmed:dateRevised	2008-11-20	lld:pubmed
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pubmed-article:12920092	pubmed:year	2003	lld:pubmed
pubmed-article:12920092	pubmed:articleTitle	Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion.	lld:pubmed
pubmed-article:12920092	pubmed:affiliation	Sezione di Genetica Medica, Dipartimento di Medicina Sperimentale e Diagnostica, Università di Ferrara, Italy.	lld:pubmed
pubmed-article:12920092	pubmed:publicationType	Journal Article	lld:pubmed
pubmed-article:12920092	pubmed:publicationType	Research Support, Non-U.S. Gov't	lld:pubmed
pubmed-article:12920092	pubmed:publicationType	Multicenter Study	lld:pubmed
entrez-gene:1756	entrezgene:pubmed	pubmed-article:12920092	lld:entrezgene
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lhgdn:association:19546	lhgdn:found_in	pubmed-article:12920092	lld:lhgdn
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