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Showing items 1-5 of 5 (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
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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
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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 |
2018-09-10T06:50:43Z |
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
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Ross, O.A. and Wu, Y.-R. and Lee, M.-C. and Funayama, M. and Chen, M.-L. and Soto, A.I. and Mata, I.F. and Lee-Chen, G.-J. and Chiung, M.C. and Tang, M. and Zhao, Y. and Hattori, N. and Farrer, M.J. and Tan, E.-K. and Wu, R.-M.; 吳逸如;李美靜;陳孟伶;李桂楨;陳瓊美;吳瑞美; Ross, Owen A.; Wu, Yih-Ru; Lee, Mei-Ching; Funayama, Manabu; Chen, Meng-Ling; Soto, Alexandra I.; Mata, Ignacio F.; Lee-Chen, Guey-Jen; Chen, Chiung Mei; Tang, Michelle; Zhao, Yi; Hattori, Nobutaka; Farrer, Matthew J.; Tan, Eng-King; Wu, Ruey-Meei; Ruey-Meei Wu; Ross, Owen A.; Wu, Yih-Ru; Lee, Mei-Ching; Funayama, Manabu; Chen, Meng-Ling; Soto, Alexandra I.; Mata, Ignacio F.; Lee-Chen, Guey-Jen; Chen, Chiung Mei; Tang, Michelle; Zhao, Yi; Hattori, Nobutaka; Farrer, Matthew J.; Tan, Eng-King; Wu, Ruey-Meei |
| 臺大學術典藏 |
2018-09-10T06:50:43Z |
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
|
Ross, O.A. and Wu, Y.-R. and Lee, M.-C. and Funayama, M. and Chen, M.-L. and Soto, A.I. and Mata, I.F. and Lee-Chen, G.-J. and Chiung, M.C. and Tang, M. and Zhao, Y. and Hattori, N. and Farrer, M.J. and Tan, E.-K. and Wu, R.-M.; 吳逸如;李美靜;陳孟伶;李桂楨;陳瓊美;吳瑞美; Ross, Owen A.; Wu, Yih-Ru; Lee, Mei-Ching; Funayama, Manabu; Chen, Meng-Ling; Soto, Alexandra I.; Mata, Ignacio F.; Lee-Chen, Guey-Jen; Chen, Chiung Mei; Tang, Michelle; Zhao, Yi; Hattori, Nobutaka; Farrer, Matthew J.; Tan, Eng-King; Wu, Ruey-Meei; Ruey-Meei Wu; Ross, Owen A.; Wu, Yih-Ru; Lee, Mei-Ching; Funayama, Manabu; Chen, Meng-Ling; Soto, Alexandra I.; Mata, Ignacio F.; Lee-Chen, Guey-Jen; Chen, Chiung Mei; Tang, Michelle; Zhao, Yi; Hattori, Nobutaka; Farrer, Matthew J.; Tan, Eng-King; Wu, Ruey-Meei |
Showing items 1-5 of 5 (1 Page(s) Totally)
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