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Nuclear FGFR2 regulates musculoskeletal integration within the developing limb
BACKGROUND: Bent Bone Dysplasia Syndrome (BBDS), a congenital skeletal disorder caused by dominant mutations in Fibroblast growth factor receptor 2 (FGFR2), is characterized by bowed long bones within the limbs. We previously showed that the FGFR2 mutations in BBDS enhance nuclear and nucleolar loca...
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| Опубликовано в: : | Dev Dyn |
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| Главные авторы: | , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2019
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6474847/ https://ncbi.nlm.nih.gov/pubmed/30620790 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvdy.9 |
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