Linked Life Data

11106359

Source:http://linkedlifedata.com/resource/pubmed/id/11106359

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2000-12-12
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1468-6244
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
37
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
E41
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:11106359-Amino Acid Sequence, pubmed-meshheading:11106359-Asian Continental Ancestry Group, pubmed-meshheading:11106359-Autistic Disorder, pubmed-meshheading:11106359-Base Sequence, pubmed-meshheading:11106359-Child, Preschool, pubmed-meshheading:11106359-Chromosomal Proteins, Non-Histone, pubmed-meshheading:11106359-Codon, Nonsense, pubmed-meshheading:11106359-DNA Mutational Analysis, pubmed-meshheading:11106359-DNA-Binding Proteins, pubmed-meshheading:11106359-Female, pubmed-meshheading:11106359-Humans, pubmed-meshheading:11106359-Infant, pubmed-meshheading:11106359-Infant, Newborn, pubmed-meshheading:11106359-Methyl-CpG-Binding Protein 2, pubmed-meshheading:11106359-Molecular Sequence Data, pubmed-meshheading:11106359-Mutation, Missense, pubmed-meshheading:11106359-Repressor Proteins, pubmed-meshheading:11106359-Rett Syndrome
pubmed:year
2000
pubmed:articleTitle
Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.
pubmed:publicationType
Letter