Case report: Whole exome sequencing and genome-wide methylation profiling of Czech dysplasia in a Chinese pedigree.

Zhao, Mengfei; Zhang, Runrun; Chang, Cen; Jin, Yehua; Xu, Lingxia; Guo, Shicheng; Schrodi, Steven; He, Yong; He, Dongyi

Zhao, Mengfei; Zhang, Runrun; Chang, Cen; Jin, Yehua; Xu, Lingxia; Guo, Shicheng; Schrodi, Steven; He, Yong; He, Dongyi.

Afiliación

Zhao M; Department of Rheumatology, Shanghai Guanghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Zhang R; High Dependency Unit, Shanghai NO.3 Rehabilitation Hospital, Shanghai, China.
Chang C; The Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, China.
Jin Y; Department of Rheumatology, The Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.
Xu L; Department of Rheumatology, Shanghai Guanghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Guo S; Arthritis Institute of Integrated Traditional and Western Medicine, Shanghai Chinese Medicine Research Institute, Shanghai, China.
Schrodi S; Department of Rheumatology, Shanghai Guanghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
He Y; Department of Rheumatology, Shanghai Guanghua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
He D; Arthritis Institute of Integrated Traditional and Western Medicine, Shanghai Chinese Medicine Research Institute, Shanghai, China.

Front Med (Lausanne) ; 10: 1244888, 2023.

Article en En | MEDLINE | ID: mdl-38020103

Palabras clave

COL2A1; Chinese pedigree; Czech dysplasia; mutation; whole exome-sequencing

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Front Med (Lausanne) Año: 2023 Tipo del documento: Article País de afiliación: China

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