Microcephaly-associated protein WDR62 supports purine metabolism by interacting with co-chaperone BAG2
Abstract Inherited mutations in the spindle pole-associated scaffold protein WDR62 cause autosomal recessive primary microcephaly. Previous research has characterised the roles of WDR62 in the regulation of spindle dynamics, cell division, and brain development. Here, we identify a new function of t...
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| Автори: | , , , , , , , , , |
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| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
Springer Nature
2026-03-01
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| Серія: | The EMBO Journal |
| Предмети: | |
| Онлайн доступ: | https://doi.org/10.1038/s44318-026-00724-0 |
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