Linked Life Data

11805248

Source:http://linkedlifedata.com/resource/pubmed/id/11805248

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2002-1-23
pubmed:abstractText
To characterize the clinical features of a new type of X-linked mental retardation associated with MECP2 mutation in the index family.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0028-3878
pubmed:author
pubmed:issnType
Print
pubmed:day
22
pubmed:volume
58
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
226-30
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed:year
2002
pubmed:articleTitle
A Rett syndrome MECP2 mutation that causes mental retardation in men.
pubmed:affiliation
Neurometabolic Unit and Center for the Diagnosis Prevention and Therapy of Neuro-handicap, University of Siena, Italy. dotti@unisi.it
pubmed:publicationType
Journal Article, Case Reports