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Hypoxia inducible factor single nucleotide polymorphisms: Exploring the role of HIF polymorphisms in retinal disease

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dc.contributor.authorThaksaon Kittipassornen_US
dc.contributor.authorDaniel J. Peeten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThe University of Adelaideen_US
dc.date.accessioned2018-11-23T11:03:44Z
dc.date.available2018-11-23T11:03:44Z
dc.date.issued2015-01-01en_US
dc.identifier.citationClinical and Experimental Ophthalmology. Vol.43, No.1 (2015), 1-2en_US
dc.identifier.doi10.1111/ceo.12493en_US
dc.identifier.issn14429071en_US
dc.identifier.issn14426404en_US
dc.identifier.other2-s2.0-84921485994en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/36778
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84921485994&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleHypoxia inducible factor single nucleotide polymorphisms: Exploring the role of HIF polymorphisms in retinal diseaseen_US
dc.typeEditorialen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84921485994&origin=inwarden_US

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