20937954

Source:http://linkedlifedata.com/resource/pubmed/id/20937954

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007758, umls-concept:C0026882, umls-concept:C0443147, umls-concept:C0450254, umls-concept:C1283195, umls-concept:C1418839, umls-concept:C1708726, umls-concept:C1858501
pubmed:issue	10
pubmed:dateCreated	2010-10-12
pubmed:abstractText	To map the disease locus and to identify a gene mutation in a Japanese family with autosomal dominant cerebellar ataxia.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372436
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins, http://linkedlifedata.com/resource/pubmed/chemical/PPP2R2B protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Protein Phosphatase 2
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	1538-3687
pubmed:author	pubmed-author:FukudaYokoY, pubmed-author:NakaharaYasuoY, pubmed-author:SasakiHidenaoH, pubmed-author:SatoKazunoriK, pubmed-author:SomaHiroyukiH, pubmed-author:TsujiShojiS, pubmed-author:YabeIchiroI
pubmed:issnType	Electronic
pubmed:volume	67
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1257-62
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:20937954-Adolescent, pubmed-meshheading:20937954-Adult, pubmed-meshheading:20937954-Cerebellar Ataxia, pubmed-meshheading:20937954-Chromosome Mapping, pubmed-meshheading:20937954-Chromosomes, Human, Pair 5, pubmed-meshheading:20937954-Family Health, pubmed-meshheading:20937954-Female, pubmed-meshheading:20937954-Genetic Linkage, pubmed-meshheading:20937954-Genome-Wide Association Study, pubmed-meshheading:20937954-Genotype, pubmed-meshheading:20937954-Humans, pubmed-meshheading:20937954-Japan, pubmed-meshheading:20937954-Magnetic Resonance Imaging, pubmed-meshheading:20937954-Male, pubmed-meshheading:20937954-Middle Aged, pubmed-meshheading:20937954-Nerve Tissue Proteins, pubmed-meshheading:20937954-Polymorphism, Single Nucleotide, pubmed-meshheading:20937954-Protein Phosphatase 2, pubmed-meshheading:20937954-Spinocerebellar Ataxias, pubmed-meshheading:20937954-Trinucleotide Repeat Expansion, pubmed-meshheading:20937954-Young Adult
pubmed:year	2010
pubmed:articleTitle	Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.
pubmed:affiliation	Department of Neurology, Graduate School of Medicine, Hokkaido University, Sapporo 060-8638, Japan.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't