Linked Life Data

12746406

Source:http://linkedlifedata.com/resource/pubmed/id/12746406

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2003-5-14
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1468-6244
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
40
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
e52
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:12746406-Adolescent, pubmed-meshheading:12746406-Adult, pubmed-meshheading:12746406-Age of Onset, pubmed-meshheading:12746406-Australia, pubmed-meshheading:12746406-Child, pubmed-meshheading:12746406-Child, Preschool, pubmed-meshheading:12746406-Chromosomal Proteins, Non-Histone, pubmed-meshheading:12746406-DNA Mutational Analysis, pubmed-meshheading:12746406-DNA-Binding Proteins, pubmed-meshheading:12746406-Dosage Compensation, Genetic, pubmed-meshheading:12746406-Genotype, pubmed-meshheading:12746406-Great Britain, pubmed-meshheading:12746406-Humans, pubmed-meshheading:12746406-Japan, pubmed-meshheading:12746406-Methyl-CpG-Binding Protein 2, pubmed-meshheading:12746406-Mutation, Missense, pubmed-meshheading:12746406-Phenotype, pubmed-meshheading:12746406-Repressor Proteins, pubmed-meshheading:12746406-Rett Syndrome
pubmed:year
2003
pubmed:articleTitle
Patients with the R133C mutation: is their phenotype different from patients with Rett syndrome with other mutations?
pubmed:publicationType
Letter, Research Support, Non-U.S. Gov't