9452089

Source:http://linkedlifedata.com/resource/pubmed/id/9452089

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0013264, umls-concept:C0021920, umls-concept:C0026882, umls-concept:C0031437, umls-concept:C0181586, umls-concept:C0205145, umls-concept:C0547040
pubmed:dateCreated	1999-6-30
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9215429
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary
pubmed:status	MEDLINE
pubmed:issn	1059-7794
pubmed:author	pubmed-author:FlorentinLL, pubmed-author:KekouKK, pubmed-author:MetaxotouCC
pubmed:issnType	Print
pubmed:volume	Suppl 1
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	S209-12
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:9452089-Adolescent, pubmed-meshheading:9452089-Alternative Splicing, pubmed-meshheading:9452089-Amino Acid Sequence, pubmed-meshheading:9452089-Base Sequence, pubmed-meshheading:9452089-Child, Preschool, pubmed-meshheading:9452089-DNA, pubmed-meshheading:9452089-DNA, Complementary, pubmed-meshheading:9452089-DNA Mutational Analysis, pubmed-meshheading:9452089-Family Health, pubmed-meshheading:9452089-Female, pubmed-meshheading:9452089-Frameshift Mutation, pubmed-meshheading:9452089-Humans, pubmed-meshheading:9452089-Infant, pubmed-meshheading:9452089-Introns, pubmed-meshheading:9452089-Male, pubmed-meshheading:9452089-Muscular Dystrophies, pubmed-meshheading:9452089-Mutation, pubmed-meshheading:9452089-Pedigree, pubmed-meshheading:9452089-Point Mutation
pubmed:year	1998
pubmed:articleTitle	3' Acceptor splice site mutation in intron 50 leads to mild Duchenne muscular dystrophy phenotype.
pubmed:affiliation	1st Department of Pediatrics, Athens University, Aghia Sophia Children's Hospital, Greece.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't