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A common FGFR3 mutation functions as a diagnostic marker for achondroplasia-group disorders in the Japanese population

✍ Scribed by Yoshito Matsui; Tomoatsu Kimura; Noriyuki Tsumaki; Haruhiko Nakahara; Nobuhito Araki; Natsuo Yasui; Takahiro Ochi

No coin nor oath required. For personal study only.

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