[3P-0370] Deficiency and overexpression of Peg11/Rtl1 in the mouse cause distinct muscle abnormalities related to Temple and Ogata-Kagami syndromes

○Moe Kitazawa¹, Shinichiro Hayashi², Michihiro Imamura³, Shin'ichi Takeda³, Yumiko Oishi⁴, Tomoko Kaneko-Ishino⁵, Fumitoshi Ishino¹ (1.Dept.of Epigenetics, MRI, TMDU, 2.Dept. of Neuromuscular Res., NCNP, 3.Dept. of Mol. Thera., NCNP, 4.Dept. of Bioc. and Mol. Biol., Nippon Med. Sch., 5.Sch. of Med., Tokai Univ.)

Peg11/Rtl1, fetal/neonatal, skeletal muscle, development, imprinting disease