Genome-wide screening of mouse knockouts reveals novel genes required for normal integumentary and oculocutaneous structure and function

Oculocutaneous syndromes are often due to mutations in single genes. In some cases, mouse models for these diseases exist in spontaneously occurring mutations, or in mice resulting from forward mutatagenesis screens. Here we present novel genes that may be causative for oculocutaneous disease in hum...

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Detalles Bibliográficos
Autores principales: Moore, Bret A., Flenniken, Ann M., Clary, Dave, Moshiri, Ata S., Nutter, Lauryl M. J., Berberovic, Zorana, Owen, Celeste, Newbigging, Susan, Adissu, Hibret, Eskandarian, Mohammad, McKerlie, Colin, Thomasy, Sara M., Lloyd, K. C. Kent, Murphy, Christopher J., Moshiri, Ala
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6672016/
https://www.ncbi.nlm.nih.gov/pubmed/31371754
http://dx.doi.org/10.1038/s41598-019-47286-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6672016/
https://www.ncbi.nlm.nih.gov/pubmed/31371754
http://dx.doi.org/10.1038/s41598-019-47286-2

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