7564249

Source:http://linkedlifedata.com/resource/pubmed/id/7564249

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015295, umls-concept:C0019880, umls-concept:C0021920, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0392760, umls-concept:C0678226, umls-concept:C0684224, umls-concept:C0751202, umls-concept:C1442161, umls-concept:C1513380
pubmed:issue	2
pubmed:dateCreated	1995-11-22
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7910918
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Cystathionine beta-Synthase
pubmed:status	MEDLINE
pubmed:issn	0141-8955
pubmed:author	pubmed-author:AndriaGG, pubmed-author:CanditoMM, pubmed-author:KrausJ PJP, pubmed-author:PanicoMM, pubmed-author:PepeAA, pubmed-author:SebastioGG, pubmed-author:SperandeoM PMP, pubmed-author:de FranchisRR
pubmed:issnType	Print
pubmed:volume	18
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	211-4
pubmed:dateRevised	2007-3-21
pubmed:meshHeading	pubmed-meshheading:7564249-Base Sequence, pubmed-meshheading:7564249-Cystathionine beta-Synthase, pubmed-meshheading:7564249-Europe, pubmed-meshheading:7564249-Exons, pubmed-meshheading:7564249-Homocystinuria, pubmed-meshheading:7564249-Humans, pubmed-meshheading:7564249-Introns, pubmed-meshheading:7564249-Molecular Sequence Data, pubmed-meshheading:7564249-Mutation, pubmed-meshheading:7564249-Repetitive Sequences, Nucleic Acid, pubmed-meshheading:7564249-Sequence Deletion
pubmed:year	1995
pubmed:articleTitle	Molecular analysis of patients affected by homocystinuria due to cystathionine beta-synthase deficiency: report of a new mutation in exon 8 and a deletion in intron 11.
pubmed:affiliation	Department of Pediatrics, Federico II University, Naples, Italy.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't