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FGFR3 Heterodimerization in Achondroplasia, the Most Common Form of Human Dwarfism
The G380R mutation in the transmembrane domain of fibroblast growth factor receptor 3 (FGFR3) causes achondroplasia, the most common form of human dwarfism. Achondroplasia is a heterozygous disorder, and thus the affected individuals express both wild-type and mutant FGFR3. Yet heterodimerization in...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Biochemistry and Molecular Biology
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3075674/ https://ncbi.nlm.nih.gov/pubmed/21324899 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M110.205583 |
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