Published in
Public Library of Science, PLoS Genetics, 2(15), p. e1007917, 2019
DOI: 10.1371/journal.pgen.1007917
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Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation
Journal article published in 2019 by
Amy E. O’Connell 
,
Maxim V. Gerashchenko ,
Marie-Francoise O’Donohue ,
Samantha M. Rosen,
Eric Huntzinger ,
Diane Gleeson ,
Antonella Galli,
Edward Ryder ,
Siqi Cao,
Quinn Murphy,
Shideh Kazerounian,
Sarah U. Morton ,
Klaus Schmitz-Abe,
Vadim N. Gladyshev,
Pierre-Emmanuel Gleizes
and other authors.
,
Maxim V. Gerashchenko ,
Marie-Francoise O’Donohue ,
Samantha M. Rosen,
Eric Huntzinger ,
Diane Gleeson ,
Antonella Galli,
Edward Ryder ,
Siqi Cao,
Quinn Murphy,
Shideh Kazerounian,
Sarah U. Morton ,
Klaus Schmitz-Abe,
Vadim N. Gladyshev,
Pierre-Emmanuel Gleizes
and other authors.
This paper is made freely available by the publisher.
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