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TJP2 hepatobiliary disorders: Novel variants and clinical diversity.
Zhang, Jing; Liu, Lang-Li; Gong, Jing-Yu; Hao, Chen-Zhi; Qiu, Yi-Ling; Lu, Yi; Feng, Jia-Yan; Li, Jia-Qi; Li, Zhong-Die; Wang, Meng-Xuan; Xing, Qing-He; Knisely, A S; Wang, Jian-She.
Afiliación
  • Zhang J; The Department of Pediatrics, Jinshan Hospital of Fudan University, Shanghai, China.
  • Liu LL; The Center for Liver Diseases, Children's Hospital of Fudan University, Shanghai, China.
  • Gong JY; The Department of Pediatrics, Jinshan Hospital of Fudan University, Shanghai, China.
  • Hao CZ; The Center for Liver Diseases, Children's Hospital of Fudan University, Shanghai, China.
  • Qiu YL; The Department of Pediatrics, Jinshan Hospital of Fudan University, Shanghai, China.
  • Lu Y; The Center for Liver Diseases, Children's Hospital of Fudan University, Shanghai, China.
  • Feng JY; The Department of Pediatrics, Jinshan Hospital of Fudan University, Shanghai, China.
  • Li JQ; The Center for Liver Diseases, Children's Hospital of Fudan University, Shanghai, China.
  • Li ZD; The Center for Liver Diseases, Children's Hospital of Fudan University, Shanghai, China.
  • Wang MX; The Department of Pathology, Children's Hospital of Fudan University, Shanghai, China.
  • Xing QH; The Department of Pediatrics, Jinshan Hospital of Fudan University, Shanghai, China.
  • Knisely AS; The Center for Liver Diseases, Children's Hospital of Fudan University, Shanghai, China.
  • Wang JS; The Department of Pediatrics, Jinshan Hospital of Fudan University, Shanghai, China.
Hum Mutat ; 41(2): 502-511, 2020 02.
Article en En | MEDLINE | ID: mdl-31696999
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Variación Genética / Colestasis Intrahepática / Predisposición Genética a la Enfermedad / Proteína de la Zonula Occludens-2 Límite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Variación Genética / Colestasis Intrahepática / Predisposición Genética a la Enfermedad / Proteína de la Zonula Occludens-2 Límite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos