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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...

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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

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