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Molecular consequences of PQBP1 deficiency, involved in t... | ResearchHub
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Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome
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Authors
Jérémie Courraud
18 more
Jérémie Courraud
•
Brigitte Gilbert‐Dussardier
16 more
•
Amélie Piton
Published
May 30, 2022
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Preprint Server
Topics
Biology
Genetics And Genomics
Nonsense-Mediated Decay
Gene Isoform
Alternative Splicing
Show all topics
DOI
10.1101/2022.05.29.493091
License
CC-BY
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Genetics And Genomics
Nonsense-Mediated Decay
Gene Isoform
Alternative Splicing
Show all topics
DOI
10.1101/2022.05.29.493091
License
CC-BY
Other Formats
PDF
