4776531

Source:http://linkedlifedata.com/resource/pubmed/id/4776531

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019425, umls-concept:C0020792, umls-concept:C0023522, umls-concept:C0036161, umls-concept:C0039373, umls-concept:C0149676, umls-concept:C0205419, umls-concept:C0439658, umls-concept:C0439858, umls-concept:C0728826, umls-concept:C1742737
pubmed:issue	1
pubmed:dateCreated	1974-4-3
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7607154
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Acid Phosphatase, http://linkedlifedata.com/resource/pubmed/chemical/Galactosidases, http://linkedlifedata.com/resource/pubmed/chemical/Hexosaminidases, http://linkedlifedata.com/resource/pubmed/chemical/Sulfatases
pubmed:status	MEDLINE
pubmed:issn	0018-7348
pubmed:author	pubmed-author:HarzerKK
pubmed:issnType	Print
pubmed:volume	20
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	9-24
pubmed:dateRevised	2009-10-27
pubmed:meshHeading	pubmed-meshheading:4776531-Acid Phosphatase, pubmed-meshheading:4776531-Adolescent, pubmed-meshheading:4776531-Adult, pubmed-meshheading:4776531-Child, pubmed-meshheading:4776531-Child, Preschool, pubmed-meshheading:4776531-Galactosidases, pubmed-meshheading:4776531-Genotype, pubmed-meshheading:4776531-Heterozygote, pubmed-meshheading:4776531-Hexosaminidases, pubmed-meshheading:4776531-Humans, pubmed-meshheading:4776531-Infant, pubmed-meshheading:4776531-Isoelectric Focusing, pubmed-meshheading:4776531-Leukocytes, pubmed-meshheading:4776531-Leukodystrophy, Metachromatic, pubmed-meshheading:4776531-Lipidoses, pubmed-meshheading:4776531-Lysosomes, pubmed-meshheading:4776531-Mathematics, pubmed-meshheading:4776531-Middle Aged, pubmed-meshheading:4776531-Pedigree, pubmed-meshheading:4776531-Phenotype, pubmed-meshheading:4776531-Sulfatases
pubmed:year	1973
pubmed:articleTitle	Inheritance of the enzyme deficiency in three neurolipidoses: variant 0 of Tay-Sachs disease (Sandhoff's disease), classic Tay-Sachs disease, and metachromatic leukodystrophy. Identification of the heterozygous carriers.
pubmed:publicationType	Journal Article, Comparative Study