[Genetic analysis of a child with ectodermal dysplasia caused by variant of EDA gene].

Ye, J H; Li, D M; Lyu, T; Zhao, W J; Guo, J J; He, J; Zhu, B S

Ye, J H; Li, D M; Lyu, T; Zhao, W J; Guo, J J; He, J; Zhu, B S.

Afiliación

Ye JH; Department of Medical Genetics, the First people's Hospital of Yunnan Province, the Affiliated Hospital of Kunming University of Science and Technology,Yunnan Provincial Clinical Medicine Research Center for Birth Defects and Rare Diseases, Kunming 650032, China.
Li DM; Department of Medical Genetics, the First people's Hospital of Yunnan Province, the Affiliated Hospital of Kunming University of Science and Technology,Yunnan Provincial Clinical Medicine Research Center for Birth Defects and Rare Diseases, Kunming 650032, China.
Lyu T; School of Medicine, Kunming University of Science and Technology, Kunming 650500, China.
Zhao WJ; Department of Medical Genetics, the First people's Hospital of Yunnan Province, the Affiliated Hospital of Kunming University of Science and Technology,Yunnan Provincial Clinical Medicine Research Center for Birth Defects and Rare Diseases, Kunming 650032, China.
Guo JJ; Department of Medical Genetics, the First people's Hospital of Yunnan Province, the Affiliated Hospital of Kunming University of Science and Technology,Yunnan Provincial Clinical Medicine Research Center for Birth Defects and Rare Diseases, Kunming 650032, China.
He J; Department of Medical Genetics, the First people's Hospital of Yunnan Province, the Affiliated Hospital of Kunming University of Science and Technology,Yunnan Provincial Clinical Medicine Research Center for Birth Defects and Rare Diseases, Kunming 650032, China.
Zhu BS; Department of Medical Genetics, the First people's Hospital of Yunnan Province, the Affiliated Hospital of Kunming University of Science and Technology,Yunnan Provincial Clinical Medicine Research Center for Birth Defects and Rare Diseases, Kunming 650032, China.

Zhonghua Er Ke Za Zhi ; 60(8): 834-835, 2022 Aug 02.

Article en Zh | MEDLINE | ID: mdl-35922200

Asunto(s)

Displasia Ectodermal Anhidrótica Tipo 1; Displasia Ectodérmica; Niño; Displasia Ectodérmica/genética; Displasia Ectodermal Anhidrótica Tipo 1/genética; Ectodisplasinas/genética; Pruebas Genéticas; Humanos; Mutación; Linaje

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Displasia Ectodérmica / Displasia Ectodermal Anhidrótica Tipo 1 Límite: Child / Humans Idioma: Zh Revista: Zhonghua Er Ke Za Zhi Año: 2022 Tipo del documento: Article País de afiliación: China

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