The squiggle tail (squig) mutation in mice is associated with a deletion in the mesenchyme homeobox 1 (Meox1) gene

OBJECTIVE: We have taken a positional approach to assign the spontaneous squiggle tail (squig) mutation in mice to a specific gene defect. RESULTS: A large panel of backcross mice was produced and characterized to map squig to high genetic resolution on mouse Chromosome (Chr) 11. Two overlapping can...

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Detalles Bibliográficos
Autores principales: Girard, Jon P., Tomasiello, Jacqueline F., Samuel-Constanzo, Juan I., Montero, Nia, Kendra, Angelina M., King, Thomas R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9502874/
https://www.ncbi.nlm.nih.gov/pubmed/36138442
http://dx.doi.org/10.1186/s13104-022-06192-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9502874/
https://www.ncbi.nlm.nih.gov/pubmed/36138442
http://dx.doi.org/10.1186/s13104-022-06192-z

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