Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2008-1-29
pubmed:abstractText
There is a marked variation in clinical phenotypes that have been associated with mutations in FKRP, ranging from severe congenital muscular dystrophies to limb-girdle muscular dystrophy type 2I (LGMD2I).
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-11592034, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-11741828, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-12471058, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-12666124, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-12707425, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-15060126, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-15121789, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-15213246, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-15505776, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-15574464, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-15580560, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-15883334, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-16055117, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-16288869, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-16634037, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-16786213, http://linkedlifedata.com/resource/pubmed/commentcorrection/18036232-17021404
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1471-2474
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
8
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
115
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
2007
pubmed:articleTitle
LGMD2I in a North American population.
pubmed:affiliation
Program in Genomics, Children's Hospital Boston and Harvard Medical School, Boston, USA. peter.kang@childrens.harvard.edu
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural