The CHARGE syndrome-associated protein FAM172A controls AGO2 nuclear import

CHARGE syndrome is a neural crest-related disorder mainly caused by mutation of the chromatin remodeler-coding gene Alternative causes include mutation of other chromatin and/or splicing factors. One of these additional players is the poorly characterized FAM172A, which we previously found in a comp...

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Veröffentlicht in:	Life science alliance 2023-08, Vol.6 (8), p.e202302133
Hauptverfasser:	Sallis, Sephora, Bérubé-Simard, Félix-Antoine, Grondin, Benoit, Leduc, Elizabeth, Azouz, Fatiha, Bélanger, Catherine, Pilon, Nicolas
Format:	Artikel
Sprache:	eng
Schlagworte:	Active Transport, Cell Nucleus CHARGE Syndrome Chromatin Humans Mutation, Missense Proteins
Online-Zugang:	Volltext
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