A Comprehensive Review of Genetically Engineered Mouse Models for Prader-Willi Syndrome Research

Prader-Willi syndrome (PWS) is a neurogenetic multifactorial disorder caused by the deletion or inactivation of paternally imprinted genes on human chromosome 15q11-q13. The affected homologous locus is on mouse chromosome 7C. The positional conservation and organization of genes including the impri...

Descripción completa

Detalles Bibliográficos
Autores principales: Kummerfeld, Delf-Magnus, Raabe, Carsten A., Brosius, Juergen, Mo, Dingding, Skryabin, Boris V., Rozhdestvensky, Timofey S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8037846/
https://www.ncbi.nlm.nih.gov/pubmed/33807162
http://dx.doi.org/10.3390/ijms22073613

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8037846/
https://www.ncbi.nlm.nih.gov/pubmed/33807162
http://dx.doi.org/10.3390/ijms22073613

Ejemplares similares