Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2010-3-18
pubmed:abstractText
Hereditary spastic paraplegia (HSP) is a clinically and genetically heterogeneous disorder that can be an autosomal-dominant, autosomal-recessive, or X-linked disease. The most common autosomal-dominant form of the disease derives from mutations in the SPAST gene.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-10896685, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-10980739, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-11015453, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-11039577, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-11470961, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-11784824, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-11985387, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-12124993, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-12471215, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-12960222, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-1512613, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-15248095, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-16005518, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-16055926, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-16832076, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-17035675, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-17098887, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-17594340, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-17895902, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-17992088, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-18364116, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-18463901, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-18701882, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-19039240, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-19423133, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-19561033, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-19726407, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-4426134, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-7793232, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-8649538, http://linkedlifedata.com/resource/pubmed/commentcorrection/20214791-9192272
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1471-2377
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
10
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
17
pubmed:dateRevised
2010-9-30
pubmed:meshHeading
pubmed-meshheading:20214791-Adenosine Triphosphatases, pubmed-meshheading:20214791-Adolescent, pubmed-meshheading:20214791-Adult, pubmed-meshheading:20214791-Aged, pubmed-meshheading:20214791-Aged, 80 and over, pubmed-meshheading:20214791-Child, pubmed-meshheading:20214791-Estonia, pubmed-meshheading:20214791-Exons, pubmed-meshheading:20214791-Family, pubmed-meshheading:20214791-Female, pubmed-meshheading:20214791-Humans, pubmed-meshheading:20214791-INDEL Mutation, pubmed-meshheading:20214791-Male, pubmed-meshheading:20214791-Middle Aged, pubmed-meshheading:20214791-Mutation, Missense, pubmed-meshheading:20214791-Phenotype, pubmed-meshheading:20214791-Polymorphism, Single Nucleotide, pubmed-meshheading:20214791-Russia, pubmed-meshheading:20214791-Spastic Paraplegia, Hereditary, pubmed-meshheading:20214791-Young Adult
pubmed:year
2010
pubmed:articleTitle
Unique spectrum of SPAST variants in Estonian HSP patients: presence of benign missense changes but lack of exonic rearrangements.
pubmed:affiliation
Department of Neurology, University of Tartu, Estonia. Mark.Braschinsky@kliinikum.ee
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't