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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...
Tallennettuna:
| Julkaisussa: | J Dev Biol |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
MDPI
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7558312/ https://ncbi.nlm.nih.gov/pubmed/32872105 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jdb8030016 |
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