Compound heterozygous RYR1 mutations by whole exome sequencing in a family with three repeated affected fetuses with fetal akinesia. (November 2018) - Suzumori, Nobuhiro; Inagaki, Hidehito; Ohtani, Ayano; Kumagai, Kyoko; Takeda, Eri; Yoshihara, Hiroyuki; Sawada, Yuki; Inuzuka, Saki; Iwagaki, Shigenori; Takahashi, Yuichiro; Kurahashi, Hiroki; Sugiura-Ogasawara, Mayumi