A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy
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K. Arimura | H. Takashima | Y. Okamoto | I. Higuchi | O. Watanabe | Y. Inamori | Y. Sakiyama | K. Michizono | Yu-ichi Goto | Hideyuki Hatakeyama | Yoko Sangatsuda