4681915

Source:http://linkedlifedata.com/resource/pubmed/id/4681915

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0268542, umls-concept:C0332120, umls-concept:C0678942, umls-concept:C1847879
pubmed:issue	1
pubmed:dateCreated	1973-1-30
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0255562
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Ammonia, http://linkedlifedata.com/resource/pubmed/chemical/Dietary Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Ornithine Carbamoyltransferase
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	0028-4793
pubmed:author	pubmed-author:CampbellA GAG, pubmed-author:ConnH OHO, pubmed-author:RosenbergL ELE, pubmed-author:ShortE MEM, pubmed-author:SnodgrassP JPJ
pubmed:issnType	Print
pubmed:day	4
pubmed:volume	288
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	7-12
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:4681915-Adult, pubmed-meshheading:4681915-Amino Acid Metabolism, Inborn Errors, pubmed-meshheading:4681915-Ammonia, pubmed-meshheading:4681915-Biopsy, Needle, pubmed-meshheading:4681915-Diet Therapy, pubmed-meshheading:4681915-Dietary Proteins, pubmed-meshheading:4681915-Female, pubmed-meshheading:4681915-Genes, Dominant, pubmed-meshheading:4681915-Heterozygote, pubmed-meshheading:4681915-Humans, pubmed-meshheading:4681915-Infant, Newborn, pubmed-meshheading:4681915-Infant, Newborn, Diseases, pubmed-meshheading:4681915-Liver, pubmed-meshheading:4681915-Male, pubmed-meshheading:4681915-Mutation, pubmed-meshheading:4681915-Ornithine Carbamoyltransferase, pubmed-meshheading:4681915-Pedigree, pubmed-meshheading:4681915-Sex Chromosomes, pubmed-meshheading:4681915-Sex Factors
pubmed:year	1973
pubmed:articleTitle	Evidence for x-linked dominant inheritance of ornithine transcarbamylase deficiency.
pubmed:publicationType	Journal Article