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Novel mutation of the TINF2 gene resulting in severe phenotypic Revesz syndrome

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dc.contributor.authorAnusak Sakwiten_US
dc.contributor.authorDuangnate Rojanapornen_US
dc.contributor.authorPimsiri Mekjaruskulen_US
dc.contributor.authorWiboon Suriyajakryuththanaen_US
dc.contributor.authorWerasak Sasanakulen_US
dc.contributor.authorNongnuch Sirachainanen_US
dc.contributor.otherFaculty of Medicine, Ramathibodi Hospital, Mahidol Universityen_US
dc.contributor.otherMaharaj Nakhon Ratchasima Hospitalen_US
dc.date.accessioned2020-01-27T10:02:46Z
dc.date.available2020-01-27T10:02:46Z
dc.date.issued2019-03-01en_US
dc.identifier.citationPediatric Blood and Cancer. Vol.66, No.3 (2019)en_US
dc.identifier.doi10.1002/pbc.27557en_US
dc.identifier.issn15455017en_US
dc.identifier.issn15455009en_US
dc.identifier.other2-s2.0-85057450467en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/51828
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85057450467&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleNovel mutation of the TINF2 gene resulting in severe phenotypic Revesz syndromeen_US
dc.typeLetteren_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85057450467&origin=inwarden_US

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