Cecr2 mutant mice as a model for human cat eye syndrome

Cat eye syndrome (CES), a human genetic disorder caused by the inverted duplication of a region on chromosome 22, has been known since the late 1890s. Despite the significant impact this disorder has on affected individuals, models for CES have not been produced due to the difficulty of effectively...

Descripción completa

Detalles Bibliográficos
Autores principales: Dicipulo, Renée, Norton, Kacie A., Fairbridge, Nicholas A., Kibalnyk, Yana, Fox, Sabrina C., Hornberger, Lisa K., McDermid, Heather E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862319/
https://www.ncbi.nlm.nih.gov/pubmed/33542446
http://dx.doi.org/10.1038/s41598-021-82556-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862319/
https://www.ncbi.nlm.nih.gov/pubmed/33542446
http://dx.doi.org/10.1038/s41598-021-82556-y

Ejemplares similares