reference/11504150

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11504150

Outgoing Links

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bibliographicCitation	O’Connell AE, Gerashchenko MV, O’Donohue M, Rosen SM, Huntzinger E, Gleeson D, Galli A, Ryder E, Cao S, Murphy Q, Kazerounian S, Morton SU, Schmitz-Abe K, Gladyshev VN, Gleizes P, Séraphin B, Agrawal PB. Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation. PLoS Genet. 2019 Feb 01;15(2):e1007917. doi: 10.1371/journal.pgen.1007917.
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source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation
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