Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2003-1-28
pubmed:abstractText
Three causative genes have been identified for autosomal dominant AD.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1526-632X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
28
pubmed:volume
60
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
235-9
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:12552037-Adult, pubmed-meshheading:12552037-Age of Onset, pubmed-meshheading:12552037-Alzheimer Disease, pubmed-meshheading:12552037-Amino Acid Substitution, pubmed-meshheading:12552037-Amyloid beta-Protein Precursor, pubmed-meshheading:12552037-Apolipoprotein E4, pubmed-meshheading:12552037-Apolipoproteins E, pubmed-meshheading:12552037-DNA Mutational Analysis, pubmed-meshheading:12552037-Gene Frequency, pubmed-meshheading:12552037-Genes, Dominant, pubmed-meshheading:12552037-Great Britain, pubmed-meshheading:12552037-Heterozygote, pubmed-meshheading:12552037-Homozygote, pubmed-meshheading:12552037-Humans, pubmed-meshheading:12552037-Membrane Proteins, pubmed-meshheading:12552037-Middle Aged, pubmed-meshheading:12552037-Mutation, pubmed-meshheading:12552037-Presenilin-1, pubmed-meshheading:12552037-Presenilin-2, pubmed-meshheading:12552037-Sequence Deletion
pubmed:year
2003
pubmed:articleTitle
Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
pubmed:affiliation
Dementia Research Group, Department of Clinical Neurology, Institute of Neurology, The National Hospital for Neurology and Neurosurgery, London, UK.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't