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Keyword [Renpenning syndrome]
Result: 1 - 3 | Page: 1 of 1
1.
Molecular Pathogenesis Of Renpenning Syndrome Caused By PQBP1 Mutations
2.
Mechanistic Studies Of PQBP1 In Nuclear Import Of The Splicing Factor And MRNA Alternative Polyadenylation
3.
PQBP1 Modulates Protein Synthesis Through The Regulation Of EEF2 Phosphorylation
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