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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
Yang, TLam, CWTsang, MWTong, SFChan, LYKam, GYPoon, PMWu, XQPang, CP
Issue Date2000
Citation
Human Mutation, 2000, v. 16 n. 4, p. 375 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/148209
ISSN
1098-1004
2021 Impact Factor: 4.700
2020 SCImago Journal Rankings: 1.981

 

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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