Col11a1a Expression Is Required for Zebrafish Development

The autosomal dominant chondrodystrophies, the Stickler type 2 and Marshall syndromes, are characterized by facial abnormalities, vision deficits, hearing loss, and articular joint issues resulting from mutations in COL11A1. Zebrafish carry two copies of the Col11a1 gene, designated Col11a1a and Col...

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Detalles Bibliográficos
Autores principales: Hardy, Makenna J., Reeck, Jonathon C., Fang, Ming, Adams, Jason S., Oxford, Julia Thom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7558312/
https://www.ncbi.nlm.nih.gov/pubmed/32872105
http://dx.doi.org/10.3390/jdb8030016

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7558312/
https://www.ncbi.nlm.nih.gov/pubmed/32872105
http://dx.doi.org/10.3390/jdb8030016

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