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Multiple Developmental Defects in sox11a Mutant Zebrafish with Features of Coffin-Siris Syndrome
A previous study suggested that human Coffin-Siris syndrome is related to the mutation of SOX11. Since the homozygous SOX11 mutant mice died soon after birth, no suitable model was available for the study of the pathogenic mechanism of Coffin-Siris syndrome. To solve this problem, we generated two v...
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| Gepubliceerd in: | Int J Biol Sci |
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| Hoofdauteurs: | , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Ivyspring International Publisher
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7545714/ https://ncbi.nlm.nih.gov/pubmed/33061816 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7150/ijbs.47510 |
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