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Muenke Syndrome Mutation, FgfR3(P244R), Causes TMJ Defects
Muenke syndrome is characterized by various craniofacial deformities and is caused by an autosomal-dominant activating mutation in fibroblast growth factor receptor 3 (FGFR3(P250R)). Here, using mice carrying a corresponding mutation (FgfR3(P244R)), we determined whether the mutation affects temporo...
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| Hlavní autoři: | , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
SAGE Publications
2012
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3383850/ https://ncbi.nlm.nih.gov/pubmed/22622662 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034512449170 |
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