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Exploring the origins of neurodevelopmental proteasomopathies associated with cardiac malformations: are neural crest cells central to certain pathological mechanisms?

Neurodevelopmental proteasomopathies constitute a recently defined class of rare Mendelian disorders, arising from genomic alterations in proteasome-related genes. These alterations result in the dysfunction of proteasomes, which are multi-subunit protein complexes essential for maintaining cellular...

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Збережено в:
Бібліографічні деталі
Автори: Virginie Vignard, Alban-Elouen Baruteau, Bérénice Toutain, Sandra Mercier, Bertrand Isidor, Richard Redon, Jean-Jacques Schott, Sébastien Küry, Stéphane Bézieau, Anne H. Monsoro-Burq, Frédéric Ebstein
Формат: Artigo
Мова:Inglês
Опубліковано: Frontiers Media S.A. 2024-07-01
Серія:Frontiers in Cell and Developmental Biology
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Онлайн доступ:https://www.frontiersin.org/articles/10.3389/fcell.2024.1370905/full
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