Search Results - Lim, Kheng Seang
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DEPDC5 mutations in familial and sporadic focal epilepsy by Tsai, Meng Han, Chan, Chung Kin, Chang, Ying Chao, Yu, Y.T., Chuang, S.T., Fan, W.L., Ling, S.C., Fu, Ting Ying, Chang, Wen Neng, Liou, Chia Wei, Chuang, Yao Chung, Ng, Ching Ching, Hwang, Daw Yang, Lim, Kheng Seang
Published 2017Get full text
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Underutilization of epilepsy surgery in ASEAN countries by Thuy Le, Minh-An, Fong, Si Lei, Lim, Kheng Seang, Gunadharma, Suryani, Sejahtera, Desin Pambudi, Visudtibhan, Anannit, Chan, Derrick, Vorachit, Somchit, Chan, Samleng, Ohnmar, -, Chua, Annabell E., Cabral-Lim, Leonor, Yassin, Norazieda, Le, Viet-Thang, Tan, Chong Tin
Published 2019Get full text
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Molecular Genetic Characterization of Patients With Focal Epilepsy Using a Customized Targeted Resequencing Gene Panel by Tsai, Meng Han, Chan, Chung Kin, Chang, Ying Chao, Lin, Chih Hsiang, Liou, Chia Wei, Chang, Wen Neng, Ng, Ching Ching, Lim, Kheng Seang, Hwang, Daw Yang
Published 2018Get full text
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R54C mutation of NOTCH3 gene in the first Rungus family with CADASIL by Lim, Kheng Seang, Ai-HueyTan, Lim, Chun Shen, Chua, Kek Heng, Lee, Ping Chin, Norlisah Ramli, Giri Shan Rajahram, Fatimah Tina Hussin, Kum, Thong Wong, Meenakshi Bhattacharjee, Ng, Ching Ching
Published 2015Get full text
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Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly by Tsai, Meng Han, Muir, Alison M., Wang, Won nJing, Kang, Yi Ning, Yang, Kun Chuan, Chao, Nian Hsin, Wu, Mei Feng, Chang, Ying Chao, Porter, Brenda E., Jansen, Laura A., Sebire, Guillaume, Deconinck, Nicolas, Fan, Wen Lang, Su, Shih Chi, Chung, Wen Hung, Almanza Fuerte, Edith P., Mehaffey, Michele G., Ng, Ching Ching, Chan, Chung Kin, Lim, Kheng Seang, Leventer, Richard J., Lockhart, Paul J., Riney, Kate, Damiano, John A., Hildebrand, Michael S., Mirzaa, Ghayda M., Dobyns, William B., Berkovic, Samuel F., Scheffer, Ingrid E., Tsai, Jin Wu, Mefford, Heather C.
Published 2020Get full text
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