A novel PHF6 mutation results in enhanced exon skipping and mild Börjeson-Forssman-Lehmann syndrome

Lignende værker

• T-cell Acute Lymphoblastic Leukemia in Association with Börjeson-Forssman-Lehmann Syndrome Due to a Mutation in PHF6
  af: Chao, Mwe Mwe, et al.
  Udgivet: (2010)
• PHF6 Deletions May Cause Borjeson-Forssman-Lehmann Syndrome in Females
  af: Berland, S., et al.
  Udgivet: (2011)
• Pathogenesis of Börjeson-Forssman-Lehmann Syndrome: Insights from PHF6 Function
  af: Jahani-Asl, Arezu, et al.
  Udgivet: (2016)
• Primary hypogonadism in the Borjeson-Forssman-Lehmann syndrome.
  af: Weber, F T, et al.
  Udgivet: (1978)
• Structural and Functional Insights into the Human Börjeson-Forssman-Lehmann Syndrome-associated Protein PHF6
  af: Liu, Zhonghua, et al.
  Udgivet: (2014)