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...

Full description

Saved in:
Bibliographic Details
Published in:Development
Main Authors: Kitazawa, Moe, Hayashi, Shinichiro, Imamura, Michihiro, Takeda, Shin'ichi, Oishi, Yumiko, Kaneko-Ishino, Tomoko, Ishino, Fumitoshi
Format: Artigo
Language:Inglês
Published: The Company of Biologists Ltd 2020
Subjects:
Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC7490516/
https://ncbi.nlm.nih.gov/pubmed/32878913
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dev.185918
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items