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Gorlin Syndrome: Recent Advances in Genetic Testing and Molecular and Cellular Biological Research
Gorlin syndrome is a skeletal disorder caused by a gain of function mutation in Hedgehog (Hh) signaling. The Hh family comprises of many signaling mediators, which, through complex mechanisms, play several important roles in various stages of development. The Hh information pathway is essential for...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590212/ https://www.ncbi.nlm.nih.gov/pubmed/33066274 http://dx.doi.org/10.3390/ijms21207559 |