Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation - Archive ouverte HAL Access content directly
Journal Articles PLoS Genetics Year : 2019

Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation

Amy O’connell
  • Function : Author
Maxim Gerashchenko
  • Function : Author
Marie-Françoise O'Donohue
Samantha Rosen
  • Function : Author
Diane Gleeson
  • Function : Author
Siqi Cao
  • Function : Author
Quinn Murphy
  • Function : Author
Shideh Kazerounian
  • Function : Author
Sarah Morton
  • Function : Author
Klaus Schmitz-Abe
  • Function : Author
Vadim Gladyshev
  • Function : Author
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Origin : Publication funded by an institution

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hal-02327840 , version 1 (18-11-2020)

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Amy O’connell, Maxim Gerashchenko, Marie-Françoise O'Donohue, Samantha Rosen, Eric Huntzinger, et al.. Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation. PLoS Genetics, 2019, 15 (2), pp.e1007917. ⟨10.1371/journal.pgen.1007917⟩. ⟨hal-02327840⟩
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