Compound heterozygous RYR1 mutations by whole exome sequencing in a family with three repeated affected fetuses with fetal akinesia

Nobuhiro Suzumori, Hidehito Inagaki, Ayano Ohtani, Kyoko Kumagai, Eri Takeda, Hiroyuki Yoshihara, Yuki Sawada, Saki Inuzuka, Shigenori Iwagaki, Yuichiro Takahashi, Hiroki Kurahashi, Mayumi Sugiura-Ogasawara

研究成果: Letter

2 引用 (Scopus)

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