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A novel mutation in the SH3BP2 gene causes cherubism: case report
BACKGROUND: Cherubism is a rare hereditary multi-cystic disease of the jaws, characterized by its typical appearance in early childhood, and stabilization and remission after puberty. It is genetically transmitted in an autosomal dominant fashion and the gene coding for SH3-binding protein 2 (SH3BP2...
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
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BioMed Central
2006
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1764878/ https://www.ncbi.nlm.nih.gov/pubmed/17147794 http://dx.doi.org/10.1186/1471-2350-7-84 |