180565

Source:http://linkedlifedata.com/resource/pubmed/id/180565

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019247, umls-concept:C0024369, umls-concept:C2924406
pubmed:dateCreated	1976-9-2
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0376450
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol Esters, http://linkedlifedata.com/resource/pubmed/chemical/Peroxidase
pubmed:status	MEDLINE
pubmed:issn	0079-6441
pubmed:author	pubmed-author:HirschhornRR, pubmed-author:WeissmannGG
pubmed:issnType	Print
pubmed:volume	1
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	49-101
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:180565-Chediak-Higashi Syndrome, pubmed-meshheading:180565-Child, pubmed-meshheading:180565-Child, Preschool, pubmed-meshheading:180565-Cholesterol Esters, pubmed-meshheading:180565-Chondrocalcinosis, pubmed-meshheading:180565-Cystinosis, pubmed-meshheading:180565-Fabry Disease, pubmed-meshheading:180565-Gangliosidoses, pubmed-meshheading:180565-Gaucher Disease, pubmed-meshheading:180565-Gout, pubmed-meshheading:180565-Granulomatous Disease, Chronic, pubmed-meshheading:180565-Hepatolenticular Degeneration, pubmed-meshheading:180565-Humans, pubmed-meshheading:180565-Infant, pubmed-meshheading:180565-Infant, Newborn, pubmed-meshheading:180565-Leukodystrophy, Globoid Cell, pubmed-meshheading:180565-Leukodystrophy, Metachromatic, pubmed-meshheading:180565-Lipodystrophy, pubmed-meshheading:180565-Lysosomes, pubmed-meshheading:180565-Metabolism, Inborn Errors, pubmed-meshheading:180565-Mucopolysaccharidoses, pubmed-meshheading:180565-Niemann-Pick Diseases, pubmed-meshheading:180565-Peroxidase
pubmed:year	1976
pubmed:articleTitle	Genetic disorders of lysosomes.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S.