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Conference Paper: Identification of a CFTR founder mutations, c.3068T>G:p.I1023R, which causes protein trafficking defects in Chinese patients with cystic fibrosis

TitleIdentification of a CFTR founder mutations, c.3068T>G:p.I1023R, which causes protein trafficking defects in Chinese patients with cystic fibrosis
Authors
Leung, KCYing, DMak, CCYChen, XYXu, WYeung, KSChu, WYMok, TKGChau, SKCMcLuskey, JOng, WPTLeong, HYChan, YKYang, WChen, JHLi, AMLau, YLLee, SLChung, BHY
Issue Date2016
Citation
The 2016 Joint Meeting of the Asian Society for Pediatric Research and Faculty of Medicine Ramathibodi Hospital (ASPR 2016), Bangkok, Thailand, 9-11 November 2016. How to Cite?
DescriptionPoster Presentation: Group 1 - Genetics/Inborn Errors of Metabolism: no. G 3-2
Persistent Identifierhttp://hdl.handle.net/10722/236478

 

DC FieldValueLanguage
dc.contributor.authorLeung, KC-
dc.contributor.authorYing, D-
dc.contributor.authorMak, CCY-
dc.contributor.authorChen, XY-
dc.contributor.authorXu, W-
dc.contributor.authorYeung, KS-
dc.contributor.authorChu, WY-
dc.contributor.authorMok, TKG-
dc.contributor.authorChau, SKC-
dc.contributor.authorMcLuskey, J-
dc.contributor.authorOng, WPT-
dc.contributor.authorLeong, HY-
dc.contributor.authorChan, YK-
dc.contributor.authorYang, W-
dc.contributor.authorChen, JH-
dc.contributor.authorLi, AM-
dc.contributor.authorLau, YL-
dc.contributor.authorLee, SL-
dc.contributor.authorChung, BHY-
dc.date.accessioned2016-11-25T00:53:59Z-
dc.date.available2016-11-25T00:53:59Z-
dc.date.issued2016-
dc.identifier.citationThe 2016 Joint Meeting of the Asian Society for Pediatric Research and Faculty of Medicine Ramathibodi Hospital (ASPR 2016), Bangkok, Thailand, 9-11 November 2016.-
dc.identifier.urihttp://hdl.handle.net/10722/236478-
dc.descriptionPoster Presentation: Group 1 - Genetics/Inborn Errors of Metabolism: no. G 3-2-
dc.languageeng-
dc.relation.ispartofAsian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016-
dc.titleIdentification of a CFTR founder mutations, c.3068T>G:p.I1023R, which causes protein trafficking defects in Chinese patients with cystic fibrosis-
dc.typeConference_Paper-
dc.identifier.emailYing, D: jonson@hku.hk-
dc.identifier.emailChu, WY: chuwyy@hku.hk-
dc.identifier.emailMok, TKG: gtkmok@hku.hk-
dc.identifier.emailChau, SKC: skchau@hku.hk-
dc.identifier.emailChan, YK: ykchanc@hku.hk-
dc.identifier.emailYang, W: yangwl@hkucc.hku.hk-
dc.identifier.emailLau, YL: lauylung@hku.hk-
dc.identifier.emailLee, SL: slleem@hku.hk-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.authorityChan, YK=rp00453-
dc.identifier.authorityYang, W=rp00524-
dc.identifier.authorityLau, YL=rp00361-
dc.identifier.authorityChung, BHY=rp00473-
dc.identifier.hkuros270664-

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