20512576

Source:http://linkedlifedata.com/resource/pubmed/id/20512576

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015295, umls-concept:C0021289, umls-concept:C0025344, umls-concept:C0026882, umls-concept:C0037889, umls-concept:C0051926, umls-concept:C0205082, umls-concept:C0678227, umls-concept:C1412402, umls-concept:C1561960, umls-concept:C1948053, umls-concept:C2347804
pubmed:issue	2
pubmed:dateCreated	2011-1-11
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9107334
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Ankyrins
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1432-0584
pubmed:author	pubmed-author:EberStefanS, pubmed-author:GundelFlorianF, pubmed-author:HeepAxelA
pubmed:issnType	Electronic
pubmed:volume	90
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	231-2
pubmed:dateRevised	2011-5-5
pubmed:meshHeading	pubmed-meshheading:20512576-Ankyrins, pubmed-meshheading:20512576-Exons, pubmed-meshheading:20512576-Humans, pubmed-meshheading:20512576-Infant, Newborn, pubmed-meshheading:20512576-Infant, Newborn, Diseases, pubmed-meshheading:20512576-Male, pubmed-meshheading:20512576-Mutation, pubmed-meshheading:20512576-Spherocytosis, Hereditary
pubmed:year	2011
pubmed:articleTitle	A new ankyrin mutation (ANK1 EXON E9X) causing severe hereditary spherocytosis in the neonatal period.
pubmed:publicationType	Letter, Case Reports