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Institution Date Title Author
國家衛生研究院 2024-11-19 A dominant negative Kcnd3 F227del mutation in mice causes spinocerebellar ataxia type 22 (SCA22) by impairing ER and Golgi functioning Hung, HC;Lin, JH;Teng, YC;Kao, CH;Wang, PY;Soong, BW;Tsai, TF
國家衛生研究院 2014-09 A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG function Tsai, PC;Huang, YH;Guo, YC;Wu, HT;Lin, KP;Tsai, YS;Liao, YC;Liu, YT;Liu, TT;Kao, LS;Yet, SF;Fann, MJ;Soong, BW;Lee, YC
國家衛生研究院 2013-09 Mutational analysis of the 5′ non-coding region of GJB1 in a Taiwanese cohort with Charcot–Marie–Tooth neuropathy Tsai, PC;Chen, CH;Liu, AB;Chen, YC;Soong, BW;Lin, KP;Yet, SF;Lee, YC
中國醫藥大學 2013-07 Mutational analysis of the 5’ non-coding region of GJB1 in a Taiwanese cohort with Charcot-Marie-Tooth neuropathy (Tsai PC);(Chen CH);(Liu AB);(Chen YC);(Soong BW);(Lin KP);林秀芳(Shaw-Fang Yet);(Lee YC)*
淡江大學 2013-02 Polymorphic Ala-allele carriers at residue 1170 of HER2 associated with Parkinson's disease Wang V; Chuang, Tzu-Chao; Kao MC; Shan DE; Soong BW; Shieh TM
臺北醫學大學 2013 Sleep disruption in spinocerebellar ataxia type 3: A genetic and polysomnographic study Chi, NF;Shiao, GM;Ku, HL;Soong, BW
中國醫藥大學 2005 Expanded trinucleotide repeats in the TBP/SCA17 gene mapped to chromosome 6q27 are associated with schizophrenia Chen, CM; Lane, HY; Wu, YR; Ro, LS; Chen, FL; Hung, WL; Hou, YT; Lin, CY; Huang, SY; Chen, IC; Soong, BW; Li, ML; Hsieh-Li, HM; Su, MT; Lee-Chen, GJ
中國醫藥大學 2005 Expanded trinucleotide repeats in the TBP/SCA17 gene mapped to chromosome 6q27 are associated with schizophrenia Chen, CM; Lane, HY; Wu, YR; Ro, LS; Chen, FL; Hung, WL; Hou, YT; Lin, CY; Huang, SY; Chen, IC; Soong, BW; Li, ML; Hsieh-Li, HM; Su, MT; Lee-Chen, GJ
中國醫藥大學 1997 Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parents Chang, JG; Jong, YJ; Lin, SP; Soong, BW; Tsai, CH; Yang, TY; Chang, CP; Wang, WS

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