Phenotypic Heterogeneity in Patients with Mutations in the Mitochondrial Complex I Assembly Gene NDUFAF5
Chen, Pin‐Shiuan, Lee, Ni‐Chung, Sung, Chieh‐Ju, Liu, Ya‐Wen, Weng, Wen‐Chin, Fan, Pi‐Chuan, Lee, Wang‐Tso, Chien, Yin‐Hsiu, Wu, Chao‐Szu, Sung, Yueh‐Feng, Tsai, Ming‐Chen, Lee, Yi‐Chung, Hsueh, Hsueh‐Wen, Fan, Sabrina Mai‐Yi, Wu, Meng‐Chen, Li, Hsun, Chen, Huan‐Yun, Lin, Han‐I, Ou‐Yang, Chih‐Hsin, Hwuh, Wuh‐Liang, Lin, Chin‐Hsien
Published in Movement disorders (01.12.2023)
Published in Movement disorders (01.12.2023)
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Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-057-05) from a patient with familial parkinsonism and polyneuropathy having a heterozygous p.Y314S mutation in UQCRC1 gene
Ou-Yang, Chih-Hsin, Lin, Han-Yi, Huang, Cheng-Yen, Lin, Chin-Hsien
Published in Stem cell research (01.12.2020)
Published in Stem cell research (01.12.2020)
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In vitro genome editing rescues parkinsonism phenotypes in induced pluripotent stem cells-derived dopaminergic neurons carrying LRRK2 p.G2019S mutation
Chang, Kuo-Hsuan, Huang, Cheng-Yen, Ou-Yang, Chih-Hsin, Ho, Chang-Han, Lin, Han-Yi, Hsu, Chia-Lang, Chen, You-Tzung, Chou, Yu-Chi, Chen, Yi-Jing, Chen, Ying, Lin, Jia-Li, Wang, Ji-Kuan, Lin, Pei-Wen, Lin, Ying-Ru, Lin, Miao-Hsia, Tseng, Chi-Kang, Lin, Chin-Hsien
Published in Stem cell research & therapy (22.09.2021)
Published in Stem cell research & therapy (22.09.2021)
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Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-070-02) from a patient with neurodegeneration with brain iron accumulation (NBIA) having compound heterozygous mutations in PANK2 gene
Ou-Yang, Chih-Hsin, Tai, Chun-Hwei, Lin, Han-Yi, Huang, Cheng-Yen, Lin, Chin-Hsien
Published in Stem cell research (01.03.2021)
Published in Stem cell research (01.03.2021)
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