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...

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Detalles Bibliográficos
Autores principales: Onodera, Shoko, Nakamura, Yuriko, Azuma, Toshifumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590212/
https://www.ncbi.nlm.nih.gov/pubmed/33066274
http://dx.doi.org/10.3390/ijms21207559

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