Linked Life Data

11402105

Source:http://linkedlifedata.com/resource/pubmed/id/11402105

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2001-6-12
pubmed:abstractText
Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the X-linked methyl CpG binding protein 2 (MeCP2) gene.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0028-3878
pubmed:author
pubmed:issnType
Print
pubmed:day
12
pubmed:volume
56
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1486-95
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:11402105-Adolescent, pubmed-meshheading:11402105-Adult, pubmed-meshheading:11402105-Child, pubmed-meshheading:11402105-Child, Preschool, pubmed-meshheading:11402105-Chromosomal Proteins, Non-Histone, pubmed-meshheading:11402105-DNA Mutational Analysis, pubmed-meshheading:11402105-DNA-Binding Proteins, pubmed-meshheading:11402105-Dosage Compensation, Genetic, pubmed-meshheading:11402105-Female, pubmed-meshheading:11402105-Gene Deletion, pubmed-meshheading:11402105-Gene Rearrangement, pubmed-meshheading:11402105-Genotype, pubmed-meshheading:11402105-Humans, pubmed-meshheading:11402105-Male, pubmed-meshheading:11402105-Methyl-CpG-Binding Protein 2, pubmed-meshheading:11402105-Phenotype, pubmed-meshheading:11402105-Point Mutation, pubmed-meshheading:11402105-Repressor Proteins, pubmed-meshheading:11402105-Rett Syndrome, pubmed-meshheading:11402105-Severity of Illness Index
pubmed:year
2001
pubmed:articleTitle
MeCP2 mutations in children with and without the phenotype of Rett syndrome.
pubmed:affiliation
Research Center for Genetic Medicine, Children's National Medical Center, Washington, DC 20010, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't