21216468

Source:http://linkedlifedata.com/resource/pubmed/id/21216468

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011615, umls-concept:C0026882, umls-concept:C0035820, umls-concept:C1414547, umls-concept:C1704711
pubmed:issue	8
pubmed:dateCreated	2011-3-14
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/21216468-20947168
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7905289
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Aspartic Acid, http://linkedlifedata.com/resource/pubmed/chemical/FCER1A protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Lysine, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, IgE
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1872-9142
pubmed:author	pubmed-author:NastalekMagdalenaM, pubmed-author:NishiyamaChiharuC, pubmed-author:OkumuraKoK, pubmed-author:PotaczekDaniel PDP, pubmed-author:UndasAnettaA, pubmed-author:Wojas-PelcAnnaA
pubmed:issnType	Electronic
pubmed:volume	48
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	979-80
pubmed:meshHeading	pubmed-meshheading:21216468-Alleles, pubmed-meshheading:21216468-Amino Acid Substitution, pubmed-meshheading:21216468-Animals, pubmed-meshheading:21216468-Asian Continental Ancestry Group, pubmed-meshheading:21216468-Aspartic Acid, pubmed-meshheading:21216468-Asthma, pubmed-meshheading:21216468-Dermatitis, Atopic, pubmed-meshheading:21216468-European Continental Ancestry Group, pubmed-meshheading:21216468-Gene Frequency, pubmed-meshheading:21216468-Genetic Predisposition to Disease, pubmed-meshheading:21216468-Genotype, pubmed-meshheading:21216468-Humans, pubmed-meshheading:21216468-Lysine, pubmed-meshheading:21216468-Mutagenesis, Site-Directed, pubmed-meshheading:21216468-Mutation, pubmed-meshheading:21216468-Polymorphism, Single Nucleotide, pubmed-meshheading:21216468-Rats, pubmed-meshheading:21216468-Receptors, IgE
pubmed:year	2011
pubmed:articleTitle	Naturally occurring FCER1A N222K mutation - its ethnicity-dependent distribution and a role in atopic dermatitis.
pubmed:publicationType	Letter, Comment