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

✍ Scribed by Faouzi Baklouti; Madeleine Morinière; Amel Haj-Khélil; Madeleine Fénéant-Thibault; Henri Gruffat; Yohann Couté; Alain Ninot; Corinne Guitton; Jean Delaunay


Book ID
116304892
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
824 KB
Volume
47
Category
Article
ISSN
1079-9796

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