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 CHD7. 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...

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Detalles Bibliográficos
Autores principales: Sallis, Sephora, Bérubé-Simard, Félix-Antoine, Grondin, Benoit, Leduc, Elizabeth, Azouz, Fatiha, Bélanger, Catherine, Pilon, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2023
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205598/
https://www.ncbi.nlm.nih.gov/pubmed/37221016
http://dx.doi.org/10.26508/lsa.202302133

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205598/
https://www.ncbi.nlm.nih.gov/pubmed/37221016
http://dx.doi.org/10.26508/lsa.202302133

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