[P50] Muscular disease

[P-291] A case of severe dilated cardiomyopathy caused by compound heterozygous of FKTN gene point mutations

Naoko Shiba^1,2, AKINORI NAKAMURA^3,4, TETSUO OZAWA^5,6, KAZUHIRO KIMURA⁷, HIROHIKO MOTOKI⁷, KOICHIRO KUWAHARA⁷, MASARU NASUNO², SHIHOKO TAKEUCHI², TAKENORI NATSUME², TOSHIMITSU YANAGISAWA², MITSUO MOTOBAYASHI², TETSUHIRO FUKUYAMA⁸, YUJI INABA⁸ (1.Regenerative Science and Medicine, Shinshu University, Matsumoto, Japan, 2.Department of Pediatrics, Shinshu University, Matsumoto, Japan, 3.The third department of Medicine, Shinshu University, Matsumoto, Japan, 4.Department of Neurology, National Hospital Organization Matsumoto Medical Center)