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14598346
Source:
http://linkedlifedata.com/resource/pubmed/id/14598346
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0011155
,
umls-concept:C0017270
,
umls-concept:C0018591
,
umls-concept:C0026882
,
umls-concept:C0750572
,
umls-concept:C0936012
,
umls-concept:C1413916
,
umls-concept:C1527075
pubmed:issue
2
pubmed:dateCreated
2003-11-4
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Codon, Nonsense
,
http://linkedlifedata.com/resource/pubmed/chemical/Dopamine beta-Hydroxylase
,
http://linkedlifedata.com/resource/pubmed/chemical/RNA Splice Sites
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1552-4825
pubmed:author
pubmed-author:CubellsJoseph FJF
,
pubmed-author:GelernterJoelJ
,
pubmed-author:KöhnkeMichael DMD
,
pubmed-author:KimChun-HyungCH
,
pubmed-author:KimKwang-SooKS
,
pubmed-author:KranzlerHenry RHR
,
pubmed-author:KuivaniemiHelenaH
,
pubmed-author:PadburyJames FJF
,
pubmed-author:RobertsonDavidD
,
pubmed-author:RomeroRobertoR
,
pubmed-author:SharmaSurendraS
,
pubmed-author:ZabetianCyrus PCP
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
123A
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
190-2
pubmed:dateRevised
2008-5-21
pubmed:meshHeading
pubmed-meshheading:14598346-African Continental Ancestry Group
,
pubmed-meshheading:14598346-Chromosome Mapping
,
pubmed-meshheading:14598346-Codon, Nonsense
,
pubmed-meshheading:14598346-Dopamine beta-Hydroxylase
,
pubmed-meshheading:14598346-European Continental Ancestry Group
,
pubmed-meshheading:14598346-Gene Frequency
,
pubmed-meshheading:14598346-Haplotypes
,
pubmed-meshheading:14598346-Humans
,
pubmed-meshheading:14598346-Mutation, Missense
,
pubmed-meshheading:14598346-Point Mutation
,
pubmed-meshheading:14598346-RNA Splice Sites
,
pubmed-meshheading:14598346-United States
pubmed:year
2003
pubmed:articleTitle
A revised allele frequency estimate and haplotype analysis of the DBH deficiency mutation IVS1+2T --> C in African- and European-Americans.
pubmed:publicationType
Letter
,
Research Support, U.S. Gov't, P.H.S.
,
Research Support, U.S. Gov't, Non-P.H.S.
,
Research Support, Non-U.S. Gov't