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Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome
Craniosynostosis syndromes are autosomal dominant human skeletal diseases that result from various mutations in fibroblast growth factor receptor genes (Fgfrs). Apert syndrome (AS) is one of the most severe craniosynostosis syndromes and is associated with severe syndactyly of the hands and feet and...
Na minha lista:
| Main Authors: | , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
The National Academy of Sciences
2000
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC18954/ https://ncbi.nlm.nih.gov/pubmed/11121055 |
| Clibeanna: |
Cuir Clib Leis
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