Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2005-7-4
pubmed:abstractText
Majeed syndrome is an autosomal recessive, autoinflammatory disorder characterised by chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia. The objectives of this study were to map, identify, and characterise the Majeed syndrome causal gene and to speculate on its function and role in skin and bone inflammation.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-10383779, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-10643706, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-10678414, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-10969284, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-11138012, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-11394625, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-11533771, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-11709538, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-11795677, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-11954565, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-11973628, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-12111372, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-12376568, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-14601923, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-14632189, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-15297675, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-15317890, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-1642259, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-1686018, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-1716076, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-1872530, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-2809904, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-2976529, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-3591758, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-3728413, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-3769984, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-3859205, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-3889079, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-4001881, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-4403064, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-478042, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-5520441, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-7762577, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-8034808, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-8227103, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-8651310, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-9039502, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-9718341, http://linkedlifedata.com/resource/pubmed/commentcorrection/15994876-9781029
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1468-6244
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
42
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
551-7
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:15994876-Adult, pubmed-meshheading:15994876-Anemia, Dyserythropoietic, Congenital, pubmed-meshheading:15994876-Animals, pubmed-meshheading:15994876-Causality, pubmed-meshheading:15994876-Chronic Disease, pubmed-meshheading:15994876-Conserved Sequence, pubmed-meshheading:15994876-DNA Mutational Analysis, pubmed-meshheading:15994876-Family, pubmed-meshheading:15994876-Female, pubmed-meshheading:15994876-Genetic Linkage, pubmed-meshheading:15994876-Homozygote, pubmed-meshheading:15994876-Humans, pubmed-meshheading:15994876-Jordan, pubmed-meshheading:15994876-Male, pubmed-meshheading:15994876-Mutation, pubmed-meshheading:15994876-Nuclear Proteins, pubmed-meshheading:15994876-Organ Specificity, pubmed-meshheading:15994876-Osteomyelitis, pubmed-meshheading:15994876-Pedigree, pubmed-meshheading:15994876-Phenotype, pubmed-meshheading:15994876-Recurrence, pubmed-meshheading:15994876-Sweet Syndrome, pubmed-meshheading:15994876-Syndrome
pubmed:year
2005
pubmed:articleTitle
Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome).
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