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Showing items 1-4 of 4 (1 Page(s) Totally)
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| 臺大學術典藏 |
2021-10-29T08:05:41Z |
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy
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CHIN-HSIEN LIN; Tsai, Pei I.; Lin, Han Yi; Hattori, Nobutaka; Funayama, Manabu; Jeon, Beomseok; Sato, Kota; Abe, Koji; Mukai, Yohei; Takahashi, Yuji; Li, Yuanzhe; Nishioka, Kenya; Yoshino, Hiroyo; Daida, Kensuke; Chen, Meng Ling; Cheng, Jay; Huang, Cheng Yen; SHIOU-RU TZENG; Wu, Yen Sheng; Lai, Hsing Jung; Tsai, Hsin Hsi; RUOH-FANG YEN; NI-CHUNG LEE; Lo, Wen Chun; Hung, Yu Chien; CHIH-CHIANG CHAN; Ke, Yi Ci; CHI-CHAO CHAO; SUNG-TSANG HSIEH; Farrer, Matthew; RUEY-MEEI WU |
| 臺大學術典藏 |
2021-03-22T03:55:46Z |
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy
|
Tsai, Pei I.; Lin, Han Yi; Hattori, Nobutaka; Funayama, Manabu; Jeon, Beomseok; Sato, Kota; Abe, Koji; Mukai, Yohei; Takahashi, Yuji; Li, Yuanzhe; Nishioka, Kenya; Yoshino, Hiroyo; Daida, Kensuke; Chen, Meng Ling; Cheng, Jay; Huang, Cheng Yen; Wu, Yen Sheng; Lai, Hsing Jung; Tsai, Hsin Hsi; Lo, Wen Chun; Hung, Yu Chien; Ke, Yi Ci; Farrer, Matthew; CHIN-HSIEN LIN; SHIOU-RU TZENG; RUOH-FANG YEN; NI-CHUNG LEE; CHIH-CHIANG CHAN; CHI-CHAO CHAO; SUNG-TSANG HSIEH; RUEY-MEEI WU |
| 臺大學術典藏 |
2020-12-10T01:14:55Z |
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy
|
Lin, Chin-Hsien;Tsai, Pei-I;Lin, Han-Yi;Hattori, Nobutaka;Funayama, Manabu;Jeon, Beomseok;Sato, Kota;Abe, Koji;Mukai, Yohei;Takahashi, Yuji;Li, Yuanzhe;Nishioka, Kenya;Yoshino, Hiroyo;Daida, Kensuke;Chen, Meng-Ling;Cheng, Jay;Huang, Cheng-Yen;Tzeng, Shiou-Ru;Wu, Yen-Sheng;Lai, Hsing-Jung;Tsai, Hsin-Hsi;Yen, Ruoh-Fang;Ni-Chung Lee;Lo, Wen-Chun;Hung, Yu-Chien;Chan, Chih-Chiang;Ke, Yi-Ci;Chao, Chi-Chao;Hsieh, Sung-Tsang;Farrer, Matthew;Wu, Ruey-Meei; Lin, Chin-Hsien; Tsai, Pei-I; Lin, Han-Yi; Hattori, Nobutaka; Funayama, Manabu; Jeon, Beomseok; Sato, Kota; Abe, Koji; Mukai, Yohei; Takahashi, Yuji; Li, Yuanzhe; Nishioka, Kenya; Yoshino, Hiroyo; Daida, Kensuke; Chen, Meng-Ling; Cheng, Jay; Huang, Cheng-Yen; Tzeng, Shiou-Ru; Wu, Yen-Sheng; Lai, Hsing-Jung; Tsai, Hsin-Hsi; Yen, Ruoh-Fang; NI-CHUNG LEE; Lo, Wen-Chun; Hung, Yu-Chien; Chan, Chih-Chiang; Ke, Yi-Ci; Chao, Chi-Chao; Hsieh, Sung-Tsang; Farrer, Matthew; Wu, Ruey-Meei |
| 臺大學術典藏 |
2020-12-10T01:14:55Z |
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy
|
Lin, Chin-Hsien;Tsai, Pei-I;Lin, Han-Yi;Hattori, Nobutaka;Funayama, Manabu;Jeon, Beomseok;Sato, Kota;Abe, Koji;Mukai, Yohei;Takahashi, Yuji;Li, Yuanzhe;Nishioka, Kenya;Yoshino, Hiroyo;Daida, Kensuke;Chen, Meng-Ling;Cheng, Jay;Huang, Cheng-Yen;Tzeng, Shiou-Ru;Wu, Yen-Sheng;Lai, Hsing-Jung;Tsai, Hsin-Hsi;Yen, Ruoh-Fang;Ni-Chung Lee;Lo, Wen-Chun;Hung, Yu-Chien;Chan, Chih-Chiang;Ke, Yi-Ci;Chao, Chi-Chao;Hsieh, Sung-Tsang;Farrer, Matthew;Wu, Ruey-Meei; Lin, Chin-Hsien; Tsai, Pei-I; Lin, Han-Yi; Hattori, Nobutaka; Funayama, Manabu; Jeon, Beomseok; Sato, Kota; Abe, Koji; Mukai, Yohei; Takahashi, Yuji; Li, Yuanzhe; Nishioka, Kenya; Yoshino, Hiroyo; Daida, Kensuke; Chen, Meng-Ling; Cheng, Jay; Huang, Cheng-Yen; Tzeng, Shiou-Ru; Wu, Yen-Sheng; Lai, Hsing-Jung; Tsai, Hsin-Hsi; Yen, Ruoh-Fang; NI-CHUNG LEE; Lo, Wen-Chun; Hung, Yu-Chien; Chan, Chih-Chiang; Ke, Yi-Ci; Chao, Chi-Chao; Hsieh, Sung-Tsang; Farrer, Matthew; Wu, Ruey-Meei |
Showing items 1-4 of 4 (1 Page(s) Totally)
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