Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2001-6-12
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
38
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
328-33
pubmed:dateRevised
2008-11-20
pubmed:meshHeading
pubmed-meshheading:11403042-Asian Continental Ancestry Group, pubmed-meshheading:11403042-Calcium Channels, pubmed-meshheading:11403042-Chromosome Mapping, pubmed-meshheading:11403042-Chromosomes, Human, pubmed-meshheading:11403042-Consanguinity, pubmed-meshheading:11403042-Founder Effect, pubmed-meshheading:11403042-Gene Frequency, pubmed-meshheading:11403042-Genetic Predisposition to Disease, pubmed-meshheading:11403042-Haplotypes, pubmed-meshheading:11403042-Humans, pubmed-meshheading:11403042-Japan, pubmed-meshheading:11403042-Linkage Disequilibrium, pubmed-meshheading:11403042-Microsatellite Repeats, pubmed-meshheading:11403042-Mutation, pubmed-meshheading:11403042-Polymorphism, Genetic, pubmed-meshheading:11403042-Software, pubmed-meshheading:11403042-Spinocerebellar Ataxias, pubmed-meshheading:11403042-Trinucleotide Repeat Expansion
pubmed:year
2001
pubmed:articleTitle
Predisposing chromosome for spinocerebellar ataxia type 6 (SCA6) in Japanese.
pubmed:publicationType
Letter, Research Support, Non-U.S. Gov't