Yin, X. ., Lin, J. ., Cao, L. ., Zhang, T. ., Zeng, S. ., Zhang, K. ., … Tang, B. . (2018). Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene. Human Molecular Genetics. https://doi.org/10.1093/hmg/ddy025 (Original work published 2018)
K Xia
First name:
K
Last name:
Xia
Zou, Y. ., He, W. ., Wang, K. ., Han, H. ., Xiao, T. ., Chen, X. ., … Zhang, Z. . (2018). Identification of rare RTN3 variants in Alzheimer’s disease in Han Chinese. Human Genetics. https://doi.org/10.1007/s00439-018-1868-1 (Original work published 2018)
Pakhrin, P. ., Xie, Y. ., Hu, Z. ., Li, X. ., Liu, L. ., Huang, S. ., … Zhang, R. . (2018). Genotype-phenotype correlation and frequency of distribution in a cohort of Chinese Charcot-Marie-Tooth patients associated with GDAP1 mutations. Journal of Neurology. https://doi.org/10.1007/s00415-018-8743-9 (Original work published 2018)