Premature Vertebral Mineralization in hmx1-Mutant Zebrafish

H6 family homeobox 1 (HMX1) regulates multiple aspects of craniofacial development, and mutations in HMX1 are linked to an ocular defect termed oculoauricular syndrome of Schorderet–Munier–Franceschetti (OAS) (MIM #612109). Recently, additional altered orofacial features have been reported, includin...

Descripción completa

Detalles Bibliográficos
Autores principales: El Fersioui, Younes, Pinton, Gaëtan, Allaman-Pillet, Nathalie, Schorderet, Daniel F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997757/
https://www.ncbi.nlm.nih.gov/pubmed/35406651
http://dx.doi.org/10.3390/cells11071088

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997757/
https://www.ncbi.nlm.nih.gov/pubmed/35406651
http://dx.doi.org/10.3390/cells11071088

Ejemplares similares