18458233

Source:http://linkedlifedata.com/resource/pubmed/id/18458233

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0037771, umls-concept:C0314603, umls-concept:C0439660, umls-concept:C0522498, umls-concept:C1415782, umls-concept:C1514623, umls-concept:C1516451, umls-concept:C1524003, umls-concept:C1551336
pubmed:issue	19
pubmed:dateCreated	2008-5-6
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Triphosphatases, http://linkedlifedata.com/resource/pubmed/chemical/Chaperonin 60, http://linkedlifedata.com/resource/pubmed/chemical/Genetic Markers, http://linkedlifedata.com/resource/pubmed/chemical/SPAST protein, human
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	1526-632X
pubmed:author	pubmed-author:DaltonAA, pubmed-author:HewamaddumaC A ACA, pubmed-author:KershawCC, pubmed-author:KirbyJJ, pubmed-author:MartindaleJJ, pubmed-author:McDermottC JCJ, pubmed-author:ShawP JPJ
pubmed:issnType	Electronic
pubmed:day	6
pubmed:volume	70
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1717-8
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:18458233-Adenosine Triphosphatases, pubmed-meshheading:18458233-Adolescent, pubmed-meshheading:18458233-Adult, pubmed-meshheading:18458233-Chaperonin 60, pubmed-meshheading:18458233-Chromosome Disorders, pubmed-meshheading:18458233-DNA Mutational Analysis, pubmed-meshheading:18458233-Female, pubmed-meshheading:18458233-Gene Frequency, pubmed-meshheading:18458233-Genes, Dominant, pubmed-meshheading:18458233-Genetic Markers, pubmed-meshheading:18458233-Genetic Predisposition to Disease, pubmed-meshheading:18458233-Genetic Testing, pubmed-meshheading:18458233-Genotype, pubmed-meshheading:18458233-Humans, pubmed-meshheading:18458233-Male, pubmed-meshheading:18458233-Mutation, pubmed-meshheading:18458233-Pedigree, pubmed-meshheading:18458233-Spastic Paraplegia, Hereditary
pubmed:year	2008
pubmed:articleTitle	HSP60 is a rare cause of hereditary spastic paraparesis, but may act as a genetic modifier.
pubmed:affiliation	Academic Neurology Unit, Medical School, Beech Hill Road, University of Sheffield, S10 2RX, UK. channa.hewamadduma@sth.nhs.uk
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't