A recurrent de novo <i>FAM111A</i> mutation causes kenny–caffey syndrome type 2
Tsuyoshi Isojima(The University of Tokyo), Sachiko Kitanaka(The University of Tokyo), Jun Yoshimura(The University of Tokyo), Etsuro Tokuhiro, Jun Mitsui(The University of Tokyo), Reiko Horikawa(National Center For Child Health and Development), Shinichi Morishita(The University of Tokyo), Akihiro Yasoda, Shoji Tsuji(The University of Tokyo), Yoichiro Oda, Koichiro Doi(The University of Tokyo), Tohru Yorifuji(Osaka City General Hospital), Hiroyuki Ishiura(The University of Tokyo)
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