Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation
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Journal Articles
PLoS Genetics
Year : 2019
Marie-Françoise O'Donohue : Connect in order to contact the contributor
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Submitted on : Wednesday, November 18, 2020-11:05:08 PM
Last modification on : Wednesday, October 30, 2024-9:45:29 PM
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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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