Novel hereditary spherocytosis-associated splice site mutation in the ANK1 gene caused by parental gonosomal mosaicism

Lignende værker

• Identification of a novel de novo ANK1 R1426* nonsense mutation in a Chinese family with hereditary spherocytosis by NGS
  af: Wang, Xiong, et al.
  Udgivet: (2017)
• An ANK1 IVS3-2A>C mutation causes exon 4 skipping in two patients from a Chinese family with hereditary spherocytosis
  af: Wang, Xiong, et al.
  Udgivet: (2017)
• A de novo ANK1 mutation associated to hereditary spherocytosis: a case report
  af: Huang, Ti-Long, et al.
  Udgivet: (2019)
• Two novel ANK1 loss‐of‐function mutations in Chinese families with hereditary spherocytosis
  af: Hao, Lili, et al.
  Udgivet: (2019)
• Novel compound heterozygous mutations in the SPTA1 gene, causing hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice
  af: Wang, Xiong, et al.
  Udgivet: (2019)