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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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| 出版年: | Dev Dyn |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2019
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| 主題: | |
| オンライン･アクセス: | 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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