21103842

Source:http://linkedlifedata.com/resource/pubmed/id/21103842

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002726, umls-concept:C0010495, umls-concept:C0061187, umls-concept:C0348026, umls-concept:C0439660, umls-concept:C1533148, umls-concept:C1556094
pubmed:issue	2
pubmed:dateCreated	2011-3-8
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370310
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Gelsolin
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	0001-5555
pubmed:author	pubmed-author:AndoYukioY, pubmed-author:AsahinaAkihikoA, pubmed-author:HasegawaKazukoK, pubmed-author:OhshimaNoboruN, pubmed-author:SaitoIkuoI, pubmed-author:TadokoroEtsukoE, pubmed-author:UedaMitsuharuM, pubmed-author:YokoyamaTeruoT
pubmed:issnType	Print
pubmed:volume	91
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	201-3
pubmed:meshHeading	pubmed-meshheading:21103842-Aged, pubmed-meshheading:21103842-Amyloidosis, Familial, pubmed-meshheading:21103842-Cutis Laxa, pubmed-meshheading:21103842-Elastic Tissue, pubmed-meshheading:21103842-Gelsolin, pubmed-meshheading:21103842-Humans, pubmed-meshheading:21103842-Male, pubmed-meshheading:21103842-Mutation, pubmed-meshheading:21103842-Skin
pubmed:year	2011
pubmed:articleTitle	Hereditary gelsolin amyloidosis: a new Japanese case with cutis laxa as a diagnostic clue.
pubmed:publicationType	Letter, Case Reports