Beta-thalassemia resulting from a single nucleotide substitution in an acceptor splice site.

Ítems similars

• Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intron.
  per: Metherall, J E, et al.
  Publicat: (1986)
• "Silent" nucleotide substitution in a beta+-thalassemia globin gene activates splice site in coding sequence RNA.
  per: Goldsmith, M E, et al.
  Publicat: (1983)
• beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site.
  per: Antonarakis, S E, et al.
  Publicat: (1984)
• Identification of a beta-thalassemia mutation associated with a novel haplotype of RFLPs.
  per: Atweh, G F, et al.
  Publicat: (1986)
• Single‐nucleotide substitution T to A in the polypyrimidine stretch at the splice acceptor site of intron 9 causes exon 10 skipping in the ACAT1 gene
  per: Sasai, Hideo, et al.
  Publicat: (2017)