10563637

Source:http://linkedlifedata.com/resource/pubmed/id/10563637

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0242960, umls-concept:C1524062, umls-concept:C1708726, umls-concept:C1858712, umls-concept:C1863704
pubmed:issue	8
pubmed:dateCreated	1999-11-30
pubmed:abstractText	To map the gene responsible for autosomal dominant pure hereditary spastic paraplegia (ADPHSP) in a large affected family.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0028-3878
pubmed:author	pubmed-author:DearloveA MAM, pubmed-author:ReidEE, pubmed-author:RhodesMM, pubmed-author:RubinszteinD CDC, pubmed-author:WhitefordM LML
pubmed:issnType	Print
pubmed:day	10
pubmed:volume	53
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1844-9
pubmed:dateRevised	2008-11-21
pubmed:meshHeading	pubmed-meshheading:10563637-Adult, pubmed-meshheading:10563637-Chromosome Mapping, pubmed-meshheading:10563637-Chromosomes, Human, Pair 8, pubmed-meshheading:10563637-Female, pubmed-meshheading:10563637-Genes, Dominant, pubmed-meshheading:10563637-Genetic Variation, pubmed-meshheading:10563637-Humans, pubmed-meshheading:10563637-Lod Score, pubmed-meshheading:10563637-Male, pubmed-meshheading:10563637-Middle Aged, pubmed-meshheading:10563637-Paraplegia, pubmed-meshheading:10563637-Pedigree, pubmed-meshheading:10563637-Phenotype
pubmed:year	1999
pubmed:articleTitle	Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity.
pubmed:affiliation	Department of Medical Genetics, University of Cambridge, UK.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't