9501271

Source:http://linkedlifedata.com/resource/pubmed/id/9501271

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0162735, umls-concept:C0205307, umls-concept:C0231220, umls-concept:C0268542, umls-concept:C0441655, umls-concept:C1533691
pubmed:issue	1
pubmed:dateCreated	1998-4-23
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7910918
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Histidine, http://linkedlifedata.com/resource/pubmed/chemical/Ornithine Carbamoyltransferase, http://linkedlifedata.com/resource/pubmed/chemical/Proline
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	0141-8955
pubmed:author	pubmed-author:FreisingerPP, pubmed-author:HässlerAA, pubmed-author:PontzB FBF, pubmed-author:StaudtMM, pubmed-author:WermuthBB
pubmed:issnType	Print
pubmed:volume	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	71-2
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:9501271-Child, Preschool, pubmed-meshheading:9501271-Female, pubmed-meshheading:9501271-Histidine, pubmed-meshheading:9501271-Humans, pubmed-meshheading:9501271-Liver, pubmed-meshheading:9501271-Metabolism, Inborn Errors, pubmed-meshheading:9501271-Ornithine Carbamoyltransferase, pubmed-meshheading:9501271-Ornithine Carbamoyltransferase Deficiency Disease, pubmed-meshheading:9501271-Point Mutation, pubmed-meshheading:9501271-Proline
pubmed:year	1998
pubmed:articleTitle	Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activity.
pubmed:affiliation	Children's Hospital, Technical University, Munich, Germany
pubmed:publicationType	Journal Article, Case Reports