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Clinical features and the genetic analysis of KAT6B-related diseases caused by a de novo mutation of the KAT6B gene c.621+1G>A.
Yang, Yu; Zhang, Hai-Meng; Huang, Hui.
Afiliación
  • Yang Y; Department of Endocrinology, Genetics and Metabolism, Nanchang University, Children's Hospital of Nanchang University, Children's Hospital of Jiangxi Province, Nanchang, 330006, Jiangxi, China; Jiangxi Children's Genetic Metabolic Diseaseclinical Research Center, Nanchang, 330006, Jiangxi, China. Electronic address: yangyu3126@outlook.com.
  • Zhang HM; Department of Endocrinology, Genetics and Metabolism, Nanchang University, Children's Hospital of Nanchang University, Children's Hospital of Jiangxi Province, Nanchang, 330006, Jiangxi, China.
  • Huang H; Department of Endocrinology, Genetics and Metabolism, Nanchang University, Children's Hospital of Nanchang University, Children's Hospital of Jiangxi Province, Nanchang, 330006, Jiangxi, China.
Asian J Surg ; 45(2): 792-794, 2022 Feb.
Article en En | MEDLINE | ID: mdl-34969575
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Múltiples Límite: Humans Idioma: En Revista: Asian J Surg Año: 2022 Tipo del documento: Article Pais de publicación: Países Bajos
Texto completo
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Imprimir
XML
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Múltiples Límite: Humans Idioma: En Revista: Asian J Surg Año: 2022 Tipo del documento: Article Pais de publicación: Países Bajos