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Keywords: Uniqueness of fetal/neonatal muscle
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Journal Articles

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

In collection:
Human development
Moe Kitazawa, Shinichiro Hayashi, Michihiro Imamura, Shin'ichi Takeda, Yumiko Oishi, Tomoko Kaneko-Ishino, Fumitoshi Ishino
Journal: Development
Development (2020) 147 (21): dev185918.
DOI: https://doi.org/10.1242/dev.185918
Published: 2 September 2020
... an important role in fetal and neonatal skeletal muscle development. Abnormal expression of human RTL1 is the major cause of the muscle symptoms observed in Temple and Kagami-Ogata syndromes. Uniqueness of fetal/neonatal muscle Temple syndrome Kagami-Ogata syndrome Gene domestication Eutherian...
View article titled, Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to Temple and Kagami-Ogata syndromes
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Includes: Supplementary data