21204240

Source:http://linkedlifedata.com/resource/pubmed/id/21204240

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019425, umls-concept:C0024145, umls-concept:C0026882, umls-concept:C0241888, umls-concept:C0443147, umls-concept:C0678227, umls-concept:C1423837
pubmed:issue	1
pubmed:dateCreated	2011-1-4
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Monomeric GTP-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/SAMHD1 protein, human
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	1552-4833
pubmed:author	pubmed-author:CrowYanick JYJ, pubmed-author:RavenscroftJane CJC, pubmed-author:RiceGillian IGI, pubmed-author:SuriMohnishM, pubmed-author:SzynkiewiczMarcinM
pubmed:issnType	Electronic
pubmed:volume	155A
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	235-7
pubmed:meshHeading	pubmed-meshheading:21204240-Adolescent, pubmed-meshheading:21204240-Chilblains, pubmed-meshheading:21204240-Female, pubmed-meshheading:21204240-Genes, Dominant, pubmed-meshheading:21204240-Humans, pubmed-meshheading:21204240-Lupus Erythematosus, Cutaneous, pubmed-meshheading:21204240-Male, pubmed-meshheading:21204240-Middle Aged, pubmed-meshheading:21204240-Monomeric GTP-Binding Proteins, pubmed-meshheading:21204240-Mutation, pubmed-meshheading:21204240-Phenotype
pubmed:year	2011
pubmed:articleTitle	Autosomal dominant inheritance of a heterozygous mutation in SAMHD1 causing familial chilblain lupus.
pubmed:affiliation	Department of Dermatology, Nottingham University Hospitals NHS Trust, UK.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't