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Article: Novel single nucleotide polymorphisms (3203A>G and 3204C>T) in the 3' end of the mitochondrial 16S rRNA gene.

TitleNovel single nucleotide polymorphisms (3203A>G and 3204C>T) in the 3' end of the mitochondrial 16S rRNA gene.
Authors
Issue Date2000
Citation
Human Mutation, 2000, v. 16 n. 4, p. 375 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/148209
ISSN
2023 Impact Factor: 3.3
2023 SCImago Journal Rankings: 1.686

 

DC FieldValueLanguage
dc.contributor.authorYang, Ten_US
dc.contributor.authorLam, CWen_US
dc.contributor.authorTsang, MWen_US
dc.contributor.authorTong, SFen_US
dc.contributor.authorChan, LYen_US
dc.contributor.authorKam, GYen_US
dc.contributor.authorPoon, PMen_US
dc.contributor.authorWu, XQen_US
dc.contributor.authorPang, CPen_US
dc.date.accessioned2012-05-29T06:11:31Z-
dc.date.available2012-05-29T06:11:31Z-
dc.date.issued2000en_US
dc.identifier.citationHuman Mutation, 2000, v. 16 n. 4, p. 375en_US
dc.identifier.issn1098-1004en_US
dc.identifier.urihttp://hdl.handle.net/10722/148209-
dc.languageengen_US
dc.relation.ispartofHuman mutationen_US
dc.subject.mesh3' Untranslated Regions - Geneticsen_US
dc.subject.meshAdenineen_US
dc.subject.meshBase Sequenceen_US
dc.subject.meshCytosineen_US
dc.subject.meshDiabetes Mellitus, Type 2 - Geneticsen_US
dc.subject.meshGuanineen_US
dc.subject.meshHumansen_US
dc.subject.meshMitochondria - Chemistryen_US
dc.subject.meshMolecular Sequence Dataen_US
dc.subject.meshPolymorphism, Single Nucleotide - Geneticsen_US
dc.subject.meshRna, Ribosomal, 16S - Geneticsen_US
dc.subject.meshThymineen_US
dc.titleNovel single nucleotide polymorphisms (3203A>G and 3204C>T) in the 3' end of the mitochondrial 16S rRNA gene.en_US
dc.typeArticleen_US
dc.identifier.emailLam, CW:ching-wanlam@pathology.hku.hken_US
dc.identifier.authorityLam, CW=rp00260en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.pmid11013458-
dc.identifier.scopuseid_2-s2.0-0034293129en_US
dc.identifier.volume16en_US
dc.identifier.issue4en_US
dc.identifier.spage375en_US
dc.identifier.issnl1059-7794-

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