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Article: Phenotypic spectrum and molecular basis in a Chinese cohort of osteogenesis imperfecta with mutations in type I collagen

TitlePhenotypic spectrum and molecular basis in a Chinese cohort of osteogenesis imperfecta with mutations in type I collagen
Authors
To, MKTChen, PKTan, ZJShek, HTZhang, JNZhou, YPYin, SYDong, ZXGao, B
Issue Date2022
Citation
Frontiers in Genetics, section Genetics of Common and Rare Diseases, 2022 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/310155

 

DC FieldValueLanguage
dc.contributor.authorTo, MKT-
dc.contributor.authorChen, PK-
dc.contributor.authorTan, ZJ-
dc.contributor.authorShek, HT-
dc.contributor.authorZhang, JN-
dc.contributor.authorZhou, YP-
dc.contributor.authorYin, SY-
dc.contributor.authorDong, ZX-
dc.contributor.authorGao, B-
dc.date.accessioned2022-01-24T02:24:40Z-
dc.date.available2022-01-24T02:24:40Z-
dc.date.issued2022-
dc.identifier.citationFrontiers in Genetics, section Genetics of Common and Rare Diseases, 2022-
dc.identifier.urihttp://hdl.handle.net/10722/310155-
dc.languageeng-
dc.relation.ispartofFrontiers in Genetics, section Genetics of Common and Rare Diseases-
dc.titlePhenotypic spectrum and molecular basis in a Chinese cohort of osteogenesis imperfecta with mutations in type I collagen-
dc.typeArticle-
dc.identifier.emailTo, MKT: mikektto@hku.hk-
dc.identifier.emailGao, B: gaobo@hku.hk-
dc.identifier.authorityTo, MKT=rp00302-
dc.identifier.authorityGao, B=rp02012-
dc.identifier.hkuros331466-

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