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
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’ contributionsConception 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
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OAE Style
Chu ATW, Chan JCK, Fung JLF, Tang W, Lee M, Wong SM, Chung MH, Yu G, Li V, Ng CTH, Project HKG, Chung BHY. 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
AMA Style
Chu ATW, Chan JCK, Fung JLF, Tang W, Lee M, Wong SM, Chung MH, Yu G, Li V, Ng CTH, Project HKG, Chung BHY. 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 Disease and Orphan Drugs Journal. 2023; 2(3): 15. http://dx.doi.org/10.20517/rdodj.2023.28
Chicago/Turabian Style
Chu, Annie Tsz Wai, Joshua Chun Ki Chan, Jasmine Lee Fong Fung, Wenshu Tang, Mianne Lee, Sze Man Wong, Man Ho Chung, Geoffrey Yu, Vivien Li, Calvin Tik Hei Ng, Hong Kong Genome Project, Brian Hon Yin Chung. 2023. "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 Disease and Orphan Drugs Journal. 2, no.3: 15. http://dx.doi.org/10.20517/rdodj.2023.28
ACS Style
Chu, ATW.; Chan JCK.; Fung JLF.; Tang W.; Lee M.; Wong SM.; Chung MH.; Yu G.; Li V.; Ng CTH.; Project HKG.; Chung BHY. 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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