9299863

Source:http://linkedlifedata.com/resource/pubmed/id/9299863

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011155, umls-concept:C0037889, umls-concept:C0051926, umls-concept:C0205214, umls-concept:C1457869, umls-concept:C1518422, umls-concept:C1527180
pubmed:issue	4
pubmed:dateCreated	1997-10-6
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0417435
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Ankyrins
pubmed:status	MEDLINE
pubmed:issn	0390-6078
pubmed:author	pubmed-author:Di MartinoDD, pubmed-author:LanciottiMM, pubmed-author:MoriP GPG, pubmed-author:PerutelliPP, pubmed-author:ValettoAA
pubmed:issnType	Print
pubmed:volume	82
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	460-2
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:9299863-Adolescent, pubmed-meshheading:9299863-Adult, pubmed-meshheading:9299863-Ankyrins, pubmed-meshheading:9299863-Child, pubmed-meshheading:9299863-Female, pubmed-meshheading:9299863-Genes, Dominant, pubmed-meshheading:9299863-Humans, pubmed-meshheading:9299863-Infant, pubmed-meshheading:9299863-Infant, Newborn, pubmed-meshheading:9299863-Male, pubmed-meshheading:9299863-Mutation, pubmed-meshheading:9299863-Spherocytosis, Hereditary
pubmed:articleTitle	Ankyrin deficiency is the most common defect in dominant and non dominant hereditary spherocytosis.
pubmed:affiliation	G. Gaslini Children's Hospital, Genoa, Italy.
pubmed:publicationType	Journal Article