Haploinsufficiency of A20 in a Chinese child caused by loss-of-function mutations in TNFAIP3: A case report and review of the literature.

Liu, Jing; Lin, Yuese; Li, Xuandi; Ba, Hongjun; He, Xiufang; Peng, Huimin; Li, Shujuan; Zhu, Ling

Liu, Jing; Lin, Yuese; Li, Xuandi; Ba, Hongjun; He, Xiufang; Peng, Huimin; Li, Shujuan; Zhu, Ling.

Afiliación

Liu J; Department of Pediatric Cardiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Lin Y; Key Laboratory on Assisted Circulation, Ministry of Health, Guangzhou, China.
Li X; Department of Pediatric Cardiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Ba H; Key Laboratory on Assisted Circulation, Ministry of Health, Guangzhou, China.
He X; Department of Pediatric Cardiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Peng H; Key Laboratory on Assisted Circulation, Ministry of Health, Guangzhou, China.
Li S; Department of Pediatric Cardiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Zhu L; Key Laboratory on Assisted Circulation, Ministry of Health, Guangzhou, China.

Front Pediatr ; 10: 990008, 2022.

Article en En | MEDLINE | ID: mdl-36727002

Palabras clave

A20; TNFAIP3; autoinflammatory disease; children; haploinsufficiency of A20

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Front Pediatr Año: 2022 Tipo del documento: Article País de afiliación: China

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