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81 research outputs found
Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation
Author
Agrawal Pankaj B.
Barsh Gregory S. (editor)
+16Â more
Cao S. (Siqi)
Galli A. (Antonella)
Gerashchenko Maxim V.
Gladyshev Vadim N.
Gleeson D. (Diane)
Gleizes P. (Pierre-Emmanuel)
Huntzinger E. (Eric)
Kazerounian S. (Shideh)
Morton Sarah U.
Murphy Q. (Quinn)
O’Connell Amy E.
O’Donohue M. (Marie-Francoise)
Rosen Samantha M.
Ryder E. (Edward)
Schmitz-Abe K. (Klaus)
Séraphin B. (Bertrand)
Publication venue
'Public Library of Science (PLoS)'
Publication date
01/02/2019
Field of study
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