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

Rare Disease and Orphan Drugs Journal ›› 2023, Vol. 2 ›› Issue (3) : 15

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Rare Disease and Orphan Drugs Journal ›› 2023, Vol. 2 ›› Issue (3) :15 DOI: 10.20517/rdodj.2023.28

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, 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. 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 DOI:10.20517/rdodj.2023.28

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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.

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