Correction: A report and review of the recurrent c.811C > T variant and mutation spectrum of Kindler syndrome in East Asians: a diagnostic odyssey of 2 weeks versus 49 yearsDownload PDF
Correction: A report and review of the recurrent c.811C > T variant and mutation spectrum of Kindler syndrome in East Asians: a diagnostic odyssey of 2 weeks versus 49 years
1Hong Kong Genome Institute, Hong Kong Special Administrative Region, Hong Kong, China.
2Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong Special Administrative Region, Hong Kong, China.
3Department of Paediatrics and Adolescent Medicine, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.
4Division of Dermatology, Department of Medicine, Clinical School of Medicine, The University of Hong Kong, Hong Kong, China.
#Authors contributed equally and considered joint first authors.
Annie Tsz Wai Chu1,#
,
Joshua Chun Ki Chan2,#
1Hong Kong Genome Institute, Hong Kong Special Administrative Region, Hong Kong, China.
2Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong Special Administrative Region, Hong Kong, China.
3Department of Paediatrics and Adolescent Medicine, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.
4Division of Dermatology, Department of Medicine, Clinical School of Medicine, The University of Hong Kong, Hong Kong, China.
#Authors contributed equally and considered joint first authors.
Joshua Chun Ki Chan2,#
, ...
Brian Hon Yin Chung1,3
1Hong Kong Genome Institute, Hong Kong Special Administrative Region, Hong Kong, China.
2Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong Special Administrative Region, Hong Kong, China.
3Department of Paediatrics and Adolescent Medicine, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.
4Division of Dermatology, Department of Medicine, Clinical School of Medicine, The University of Hong Kong, Hong Kong, China.
#Authors contributed equally and considered joint first authors.
1Hong Kong Genome Institute, Hong Kong Special Administrative Region, Hong Kong, China.
2Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong Special Administrative Region, Hong Kong, China.
3Department of Paediatrics and Adolescent Medicine, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, Hong Kong, China.
4Division of Dermatology, Department of Medicine, Clinical School of Medicine, The University of Hong Kong, Hong Kong, China.
#Authors contributed equally and considered joint first authors.
Correspondence to: Dr. Brian Hon Yin Chung, Hong Kong Genome Institute, 2/F, Building 20E, Hong Kong Science Park, Hong Kong, China. E-mail: bhychung@genomics.org.hk
Received: 14 Aug 2023 | Accepted: 18 Aug 2023 | Published: 21 Aug 2023
Academic Editor: Daniel Scherman | Copy Editor: Dan Zhang | Production Editor: Dan Zhang
The authors wish to add Dr. Sze Man Wong as a co-author of the paper and add the Authors’ contributions in the Declaration part of the paper. The two cases reported in the paper were under Dr Wong’s care. The dermatological symptoms and signs are under vigorous dermatological verification by her, together with initiating a referral for a genetic test, as in these two reported cases. She provided details of the dermatological description, reflecting the expert input after that by dermatologists.
The authors apologize for any inconvenience caused and state that the scientific conclusions are unaffected.
DECLARATIONS
Authors’ contributions
Conception and design: Chung BHY, Chu ATW
Drafting the article: Chu ATW, Chan JCK, Fung JLF
Data analysis and interpretation: Fung JLF, Tang W, Lee M
Critical revision: Chung BHY, Chu ATW
Final approval of the version to be published: Chung BHY, Chu ATW, Chan JCK, Fung JLF, Tang W, Lee M, Wong SM, Chung MH, Yu G, Li V, Ng CTH
Patient recruitment and data collection: Hong Kong Genome Project
Cite This Article
Correction
Open Access
Correction: A report and review of the recurrent c.811C > T variant and mutation spectrum of Kindler syndrome in East Asians: a diagnostic odyssey of 2 weeks versus 49 years
Annie Tsz Wai Chu, ... Brian Hon Yin Chung
How to Cite
Chu, A. T. W.; Chan J. C. K.; Fung J. L. F.; Tang W.; Lee M.; Wong S. M.; Chung M. H.; Yu G.; Li V.; Ng C. T. H.; Project H. K. G.; Chung B. H. Y. Correction: A report and review of the recurrent c.811C > T variant and mutation spectrum of Kindler syndrome in East Asians: a diagnostic odyssey of 2 weeks versus 49 years. Rare. Dis. Orphan. Drugs. J.2023, 2, 15. http://dx.doi.org/10.20517/rdodj.2023.28
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