Whole exome sequencing revealed biallelic <i><scp>IFT122</scp></i> mutations in a family with <scp>CED1</scp> and recurrent pregnancy loss
Yoshinori Tsurusaki(Yokohama City University), Naomichi Matsumoto(Yokohama City University), Rika Yonezawa(National Cerebral and Cardiovascular Center), Gen Nishimura(Musashino University), Ritsuko K. Pooh, Mitsuko Nakashima(Hamamatsu University School of Medicine), Hirotomo Saitsu(Hamamatsu University), Mitsuko Furuya(Sapporo City General Hospital), Shigeru Saito(Shonan Kamakura General Hospital), Noriko Miyake(National Center for Global Health and Medicine)
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