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The p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosis

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dc.contributor.authorYilai Shuen_US
dc.contributor.authorLijun Wangen_US
dc.contributor.authorXiaoting Chengen_US
dc.contributor.authorChayada Tangshewinsirikulen_US
dc.contributor.authorWeili Shien_US
dc.contributor.authorYasheng Yuanen_US
dc.contributor.authorZhiqiang Yanen_US
dc.contributor.authorHuawei Lien_US
dc.contributor.authorJun Shenen_US
dc.contributor.authorBing Chenen_US
dc.contributor.authorWeiguo Zouen_US
dc.contributor.otherSchool of Life Sciences Fudan Universityen_US
dc.contributor.otherZhengzhou Universityen_US
dc.contributor.otherBrigham and Women's Hospitalen_US
dc.contributor.otherFaculty of Medicine, Ramathibodi Hospital, Mahidol Universityen_US
dc.contributor.otherFudan Universityen_US
dc.contributor.otherHarvard Medical School Center for Hereditary Deafnessen_US
dc.contributor.otherShanghai Institute for Biological Sciences Chinese Academy of Sciencesen_US
dc.date.accessioned2020-01-27T07:38:47Z
dc.date.available2020-01-27T07:38:47Z
dc.date.issued2019-09-20en_US
dc.identifier.citationJournal of Genetics and Genomics. Vol.46, No.9 (2019), 445-449en_US
dc.identifier.doi10.1016/j.jgg.2019.09.003en_US
dc.identifier.issn18735533en_US
dc.identifier.issn16738527en_US
dc.identifier.other2-s2.0-85075078839en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/50079
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85075078839&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleThe p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosisen_US
dc.typeLetteren_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85075078839&origin=inwarden_US

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