Homozygous deletion of EPB41 genuine AUG-containing exons results in mRNA splicing defects, NMD activation and protein 4.1R complete deficiency in hereditary elliptocytosis

Faouzi Baklouti, Madeleine Morinière, Amel Haj-Khélil, Madeleine Fénéant-Thibault, Henri Gruffat, Yohann Couté, Alain Ninot, Corinne Guitton, Jean Delaunay
  • Blood Cells Molecules and Diseases, October 2011, Elsevier
  • DOI: 10.1016/j.bcmd.2011.07.001

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http://dx.doi.org/10.1016/j.bcmd.2011.07.001

The following have contributed to this page: Dr Henri Gruffat