SATB2-associated syndrome caused by a novel SATB2 mutation in a Chinese boy: A case report and literature review

Gelijkaardige items

• A novel compound mutation in GLRA1 cause hyperekplexia in a Chinese boy- a case report and review of the literature
  door: Yang, Zhiliang, et al.
  Gepubliceerd in: (2017)
• Berardinelli-Seip syndrome in a Chinese boy with Seipin gene mutation: a case study and literature review of genotype-phenotype
  door: Huang, Shan, et al.
  Gepubliceerd in: (2013)
• Early-onset epilepsy and microcephaly-capillary malformation syndrome caused by a novel STAMBP mutation in a Chinese boy
  door: Wu, Fangrui, et al.
  Gepubliceerd in: (2019)
• Novel mutation in CNNM4 gene in a Chinese family with Jalili syndrome and literature review
  door: Jing Lu, et al.
  Gepubliceerd in: (2025-12-01)
• A Novel WASP Gene Mutation in a Chinese Boy with Wiskott–Aldrich Syndrome
  door: Wu, Hui, et al.
  Gepubliceerd in: (2014)