Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2009-7-28
pubmed:abstractText
Mutations in both alleles of parkin have been shown to result in Parkinson disease (PD). However, it is unclear whether haploinsufficiency (presence of a mutation in only 1 of the 2 parkin alleles) increases the risk for PD.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-10072423, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-10319889, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-10824074, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-10894217, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-11558785, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-11971093, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-1202204, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-12058349, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-12112109, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-12114481, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-12116199, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-12629236, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-15390068, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-15680455, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-16769863, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-16997464, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-17078063, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-17187375, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-17804834, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-18091429, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-18785635, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-18985386, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-5662937, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-6067254, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-7183759, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-9560156, http://linkedlifedata.com/resource/pubmed/commentcorrection/19636047-9802278
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1526-632X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
28
pubmed:volume
73
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
279-86
pubmed:dateRevised
2010-9-27
pubmed:meshHeading
pubmed-meshheading:19636047-Adolescent, pubmed-meshheading:19636047-Adult, pubmed-meshheading:19636047-Age of Onset, pubmed-meshheading:19636047-Aged, pubmed-meshheading:19636047-Aged, 80 and over, pubmed-meshheading:19636047-Base Sequence, pubmed-meshheading:19636047-DNA Mutational Analysis, pubmed-meshheading:19636047-Female, pubmed-meshheading:19636047-Gene Deletion, pubmed-meshheading:19636047-Gene Dosage, pubmed-meshheading:19636047-Gene Frequency, pubmed-meshheading:19636047-Genetic Markers, pubmed-meshheading:19636047-Genetic Predisposition to Disease, pubmed-meshheading:19636047-Genetic Testing, pubmed-meshheading:19636047-Genotype, pubmed-meshheading:19636047-Haplotypes, pubmed-meshheading:19636047-Humans, pubmed-meshheading:19636047-Male, pubmed-meshheading:19636047-Middle Aged, pubmed-meshheading:19636047-Mutation, pubmed-meshheading:19636047-Parkinson Disease, pubmed-meshheading:19636047-Point Mutation, pubmed-meshheading:19636047-Risk Factors, pubmed-meshheading:19636047-Ubiquitin-Protein Ligases, pubmed-meshheading:19636047-Young Adult
pubmed:year
2009
pubmed:articleTitle
Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations.
pubmed:affiliation
Medical and Molecular Genetics, Indiana University, School of Medicine, Hereditary Genomics Division, 410 W. 10th St., MI-4000, Indianapolis, IN 46202, USA. tforoud@iupui.edu
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural