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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Detalles Bibliográficos
Autores principales: Jia, Shaoting, Wu, Xingxing, Wu, Yunya, Cui, Xuefan, Tao, Binbin, Zhu, Zuoyan, Hu, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545714/
https://www.ncbi.nlm.nih.gov/pubmed/33061816
http://dx.doi.org/10.7150/ijbs.47510

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545714/
https://www.ncbi.nlm.nih.gov/pubmed/33061816
http://dx.doi.org/10.7150/ijbs.47510

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