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Hearing loss in a mouse model of Muenke syndrome
The heterozygous Pro250Arg substitution mutation in fibroblast growth factor receptor 3 (FGFR3), which increases ligand-dependent signalling, is the most common genetic cause of craniosynostosis in humans and defines Muenke syndrome. Since FGF signalling plays dosage-sensitive roles in the different...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2644644/ https://ncbi.nlm.nih.gov/pubmed/18818193 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn311 |
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