Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to Temple and Kagami-Ogata syndromes

Temple and Kagami-Ogata syndromes are genomic imprinting diseases caused by maternal and paternal duplication of human chromosome 14, respectively. They exhibit different postnatal muscle-related symptoms as well as prenatal placental problems. Using the mouse models for these syndromes, it has been...

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Detalles Bibliográficos
Autores principales: Kitazawa, Moe, Hayashi, Shinichiro, Imamura, Michihiro, Takeda, Shin'ichi, Oishi, Yumiko, Kaneko-Ishino, Tomoko, Ishino, Fumitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7490516/
https://www.ncbi.nlm.nih.gov/pubmed/32878913
http://dx.doi.org/10.1242/dev.185918

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7490516/
https://www.ncbi.nlm.nih.gov/pubmed/32878913
http://dx.doi.org/10.1242/dev.185918

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