Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
13
pubmed:dateCreated
2009-3-31
pubmed:abstractText
About 20% of familial amyotrophic lateral sclerosis (ALS) is caused by mutations in SOD1 and is typically transmitted as an autosomal dominant trait. However, due to reduced mutation penetrance, the disease may present in a recessive or sporadic manner.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-10976937, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-11006081, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-11464847, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-11715057, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-11731797, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-12824367, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-15122293, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-16423367, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-17486090, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-18090923, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-18424447, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-7063411, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-7647793, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-8446170, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-9021253, http://linkedlifedata.com/resource/pubmed/commentcorrection/19332692-9786240
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1526-632X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
31
pubmed:volume
72
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1153-9
pubmed:dateRevised
2010-9-22
pubmed:meshHeading
pubmed:year
2009
pubmed:articleTitle
A mechanism for low penetrance in an ALS family with a novel SOD1 deletion.
pubmed:affiliation
Centre for Neurodegenerative Diseases, Department of Medicine, University of Toronto, 6 Queen's Park Crescent West, Toronto, Ontario, Canada, M5S 3H2.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't