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Identification of a de novo mutation of the FOXG1 gene and comprehensive analysis for molecular factors in Chinese FOXG1-related encephalopathies.
Lu, Guanting; Zhang, Yan; Xia, Huiyun; He, Xiaoyan; Xu, Pei; Wu, Lianying; Li, Ding; Ma, Liya; Wu, Jin; Peng, Qiongling.
Afiliação
  • Lu G; Laboratory of Translational Medicine Research, Department of Pathology, Deyang People's Hospital, Deyang, China.
  • Zhang Y; Key Laboratory of Tumor Molecular Research of Deyang, Deyang, China.
  • Xia H; Department of Obstetrics and Gynecology, Strategic Support Force Medical Center, Beijing, China.
  • He X; Department of Child Healthcare, Shenzhen Baoan Women's and Children's Hospital, Jinan University, Shenzhen, China.
  • Xu P; Laboratory of Translational Medicine Research, Department of Pathology, Deyang People's Hospital, Deyang, China.
  • Wu L; Key Laboratory of Tumor Molecular Research of Deyang, Deyang, China.
  • Li D; Laboratory of Translational Medicine Research, Department of Pathology, Deyang People's Hospital, Deyang, China.
  • Ma L; Key Laboratory of Tumor Molecular Research of Deyang, Deyang, China.
  • Wu J; Laboratory of Translational Medicine Research, Department of Pathology, Deyang People's Hospital, Deyang, China.
  • Peng Q; Key Laboratory of Tumor Molecular Research of Deyang, Deyang, China.
Front Mol Neurosci ; 15: 1039990, 2022.
Article em En | MEDLINE | ID: mdl-36568277

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article