Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer protein
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M. Koenig | J. Mandel | M. Hamida | M. Arita | H. Arai | R. Sokol | F. Hentati | Keizō Inoue | H. Kayden | K. Ouahchi
暂无分享,去创建一个
M. Koenig | J. Mandel | M. Hamida | M. Arita | H. Arai | R. Sokol | F. Hentati | Keizō Inoue | H. Kayden | K. Ouahchi