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; 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

doi:10.20517/rdodj.2023.28

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Correction | Open Access | 20 Aug 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

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Annie Tsz Wai Chu^1,#

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Brian Hon Yin Chung^1,3

Rare Dis Orphan Drugs J 2023;2:15.

10.20517/rdodj.2023.28 | © The Author(s) 2023.

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This is a Correction of the paper published on 3 Mar 2023: 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’ 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

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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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© The Author(s) 2023. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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