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Friedreich-like ataxia with retintis pigmentosa caused by the His101Gln mutation of the α-tocopherol transfer protein gene
Takanori Yokota, Toshiaki Shiojiri, Takanari Gotoda, Makoto Arita, Hiroyuki Arai, Tatsuhide Ohga, Takashi Kanda, Junichi Suzuki, Tomihiro Imai, Hiroyuki Matsumoto, Seiyo Harino, Motohiro Kiyosawa, Hidehiro Mizusawa, Keizo Inoue
Research output: Contribution to journal › Article › peer-review
120
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(Scopus)