A case report of BCL11B mutation induced neurodevelopmental disorder and literature review
Objective: To analyze the clinical , immunological and genetic features of a child with BCL11B mutation induced neurodevelopmental disorder. Methods: The clinical data and genetic test of a child with BCL11B mutation hospitalized in the Department of Rheumatology and Immunology in Children's Ho...
Ausführliche Beschreibung
Bibliographische Detailangaben
| Veröffentlicht in: | Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 58(2020), 3 vom: 02. März, Seite 223-227
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| 1. Verfasser: |
Yan, S
(VerfasserIn) |
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| Weitere Verfasser: |
Wei, Y S,
Yang, Q Y,
Yang, L,
Zeng, T,
Tang, X M,
Zhao, X D,
An, Y F |
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| Format: | Online-Aufsatz
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| Sprache: | Chinese |
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| Veröffentlicht: |
2020
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| Zugriff auf das übergeordnete Werk: | Zhonghua er ke za zhi = Chinese journal of pediatrics
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| Schlagworte: | Case Reports
Journal Article
Review
Genes
Mutation
Nervous system
BCL11B protein, human
Repressor Proteins
Transcription Factors
Tumor Suppressor Proteins |
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