11783530

Source:http://linkedlifedata.com/resource/pubmed/id/11783530

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011155, umls-concept:C0019425, umls-concept:C0205197, umls-concept:C0205198, umls-concept:C1273518, umls-concept:C1556094, umls-concept:C2752073
pubmed:dateCreated	2002-1-9
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0121103
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/AMP Deaminase
pubmed:status	MEDLINE
pubmed:issn	0065-2598
pubmed:author	pubmed-author:GotoHH, pubmed-author:OgasawaraNN, pubmed-author:YamadaYY
pubmed:issnType	Print
pubmed:volume	486
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	71-4
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:11783530-AMP Deaminase, pubmed-meshheading:11783530-Alleles, pubmed-meshheading:11783530-Erythrocytes, pubmed-meshheading:11783530-Female, pubmed-meshheading:11783530-Gene Frequency, pubmed-meshheading:11783530-Genetic Testing, pubmed-meshheading:11783530-Heterozygote, pubmed-meshheading:11783530-Humans, pubmed-meshheading:11783530-Japan, pubmed-meshheading:11783530-Male, pubmed-meshheading:11783530-Mutation, pubmed-meshheading:11783530-Mutation, Missense, pubmed-meshheading:11783530-Pedigree, pubmed-meshheading:11783530-Point Mutation, pubmed-meshheading:11783530-Polymorphism, Restriction Fragment Length
pubmed:year	2000
pubmed:articleTitle	Erythrocyte amp deaminase deficiency in Japanese: a compound heterozygote responsible for the complete deficiency.
pubmed:affiliation	Institute for Developmental Research, Aichi Human Service Center, Kasugai, Japan.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't